(E)-3-(2-Chloro-3,3,3-trifluoro­prop-1-en­yl)-2,2-dimethyl-N-(2-naphth­yl)cyclo­propane­carboxamide

Liu, D.-Q.; Yan, F.-Y.

doi:10.1107/S1600536808032078

organic compounds

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ISSN: 2056-9890

Volume 64| Part 11| November 2008| Page o2191

doi:10.1107/S1600536808032078

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(E)-3-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-(2-naphthyl)cyclopropanecarboxamide

Dong-Qing Liu ^a ^* and Fan-Yong Yan ^a

^aSchool of Materials and Chemical Engineering, Tianjin Polytechnic University, Tianjin 300160, People's Republic of China
^*Correspondence e-mail: ldqyfy@yahoo.com.cn

(Received 24 September 2008; accepted 6 October 2008; online 25 October 2008)

The title compound, C₁₉H₁₇ClF₃NO, was synthesized from 3-[(E)-2-chloro-3,3,3-trifluoroprop-1-enyl]-2,2-dimethylcyclopropanecarboxylic acid and 2-aminonaphthalene. There are two molecules in the asymmetric unit. The dihedral angle between the naphthalene and cyclopropane units is 111.6 (5)°. Molecules are connected into chains by intermolecular N—H⋯O hydrogen bonds. One of the Cl atoms is disordered over two positions with occupancies 0.653 (15) and 0.347 (15).

Related literature

For general background, see: Punja (1981 ). For synthetic details, see: Liu & Yan (2007 ).

Experimental

Crystal data

C₁₉H₁₇ClF₃NO
M_r = 367.79
Orthorhombic, P 2₁ 2₁ 2₁
a = 9.6310 (8) Å
b = 16.9090 (16) Å
c = 22.485 (2) Å
V = 3661.6 (6) Å³
Z = 8
Mo Kα radiation
μ = 0.24 mm⁻¹
T = 113 (2) K
0.32 × 0.22 × 0.14 mm

Data collection

Rigaku Saturn diffractometer
Absorption correction: multi-scan (CrystalClear; Rigaku/MSC, 2005 ) T_min = 0.926, T_max = 0.967
34375 measured reflections
8701 independent reflections
8283 reflections with I > 2σ(I)
R_int = 0.046

Refinement

R[F² > 2σ(F²)] = 0.053
wR(F²) = 0.115
S = 1.14
8701 reflections
473 parameters
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.23 e Å⁻³
Δρ_min = −0.28 e Å⁻³
Absolute structure: Flack (1983 ), 3846 Friedel pairs
Flack parameter: −0.05 (6)

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1⋯O2	0.86 (3)	2.09 (3)	2.932 (2)	167 (2)
N2—H2A⋯O1ⁱ	0.82 (2)	2.19 (3)	3.003 (2)	169 (2)
Symmetry code: (i) x-1, y, z.

Data collection: CrystalClear (Rigaku/MSC, 2005); cell refinement: CrystalClear; data reduction: CrystalClear; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Bruker, 1997 ); software used to prepare material for publication: CrystalStructure (Rigaku/MSC, 2005).

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808032078/bt2796sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808032078/bt2796Isup2.hkl

checkCIF report

Comment top

3-[(E)-2-Chloro-3,3,3-trifluoroprop-1-enyl]-2,2-dimethylcyclopropanecarboxylic acid is a very important intermediate for tefluthrin, an important insecticide controlling a wide range of soil insect pests in maize,sugar beet, and other crops (Punja, 1981). Naphthalene is also a good structure which has bioactivity. The structure in this article containing both of two active parts may be show some insecticide activity probably. The present X-ray crystal structure analysis was undertaken in order to study the stereochemistry and crystal packing of the title compound, (I) In this paper, the title compound, (E)-3-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-(naphthalen-2-yl)cyclopropanecarboxamide, (I), was synthesized and the structure of (I) was illustrated in Fig. 1. The dihedral angles between the naphthalene moiety and the cycloprapane group is 111.6 (5)°. The amide hydrogen is linking with the amide oxygen in another molecule by an intermolecular N—H···O···H—C hydrogen bond. The packing can be described as a dimeric arrangement of molecules linked through N—H···O···H—C hydrogen bond as shown in Fig. 2 and Table 1.

Related literature top

For general background, see: Punja (1981). For synthetic details, see: Liu & Yan (2007). [Please check rephrasing]

Experimental top

The title compound was prepared according to the method of Liu & Yan (2007). The product was recrystallized from methanol and ethyl acetate (10:1) over 2 d at ambient temperature, gave colourless single crystals of (E)-3-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N- (naphthalen-2-yl)cyclopropanecarboxamide, suitable for X-ray analysis.

Computing details top

Data collection: CrystalClear (Rigaku/MSC, 2005); cell refinement: CrystalClear (Rigaku/MSC, 2005); data reduction: CrystalClear (Rigaku/MSC, 2005); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Bruker, 1997); software used to prepare material for publication: CrystalStructure (Rigaku/MSC, 2005).

Figures top

	Fig. 1. The molecular structure of (I), methanol, drawn with 30% probability ellipsoids. H atoms are drawn as spheres of arbitrary radius.
	Fig. 2. The crystal structure of (I), methanol, viewed along b axis

(E)-3-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl- N-(2-naphthyl)cyclopropanecarboxamide top

Crystal data top

C₁₉H₁₇ClF₃NO	D_x = 1.334 Mg m⁻³
M_r = 367.79	Mo Kα radiation, λ = 0.71070 Å
Orthorhombic, P2₁2₁2₁	Cell parameters from 9431 reflections
a = 9.6310 (8) Å	θ = 1.2–27.9°
b = 16.9090 (16) Å	µ = 0.24 mm⁻¹
c = 22.485 (2) Å	T = 113 K
V = 3661.6 (6) Å³	Block, colourless
Z = 8	0.32 × 0.22 × 0.14 mm
F(000) = 1520

Data collection top

Rigaku Saturn diffractometer	8701 independent reflections
Radiation source: rotating anode	8283 reflections with I > 2σ(I)
Confocal monochromator	R_int = 0.046
Detector resolution: 14.63 pixels mm^-1	θ_max = 27.9°, θ_min = 1.5°
ω scans	h = −12→12
Absorption correction: multi-scan (CrystalClear; Rigaku/MSC, 2005)	k = −22→21
T_min = 0.926, T_max = 0.967	l = −29→29
34375 measured reflections

Refinement top

Refinement on F²	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F² > 2σ(F²)] = 0.053	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.115	w = 1/[σ²(F_o²) + (0.0431P)² + 0.7651P] where P = (F_o² + 2F_c²)/3
S = 1.14	(Δ/σ)_max = 0.004
8701 reflections	Δρ_max = 0.23 e Å⁻³
473 parameters	Δρ_min = −0.28 e Å⁻³
0 restraints	Absolute structure: Flack (1983), with how many Friedel pairs?
Primary atom site location: structure-invariant direct methods	Absolute structure parameter: −0.05 (6)

Crystal data top

C₁₉H₁₇ClF₃NO	V = 3661.6 (6) Å³
M_r = 367.79	Z = 8
Orthorhombic, P2₁2₁2₁	Mo Kα radiation
a = 9.6310 (8) Å	µ = 0.24 mm⁻¹
b = 16.9090 (16) Å	T = 113 K
c = 22.485 (2) Å	0.32 × 0.22 × 0.14 mm

Data collection top

Rigaku Saturn diffractometer	8701 independent reflections
Absorption correction: multi-scan (CrystalClear; Rigaku/MSC, 2005)	8283 reflections with I > 2σ(I)
T_min = 0.926, T_max = 0.967	R_int = 0.046
34375 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.053	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.115	Δρ_max = 0.23 e Å⁻³
S = 1.14	Δρ_min = −0.28 e Å⁻³
8701 reflections	Absolute structure: Flack (1983), with how many Friedel pairs?
473 parameters	Absolute structure parameter: −0.05 (6)
0 restraints

Special details top

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.

Refinement. Refinement of F² against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F², conventional R-factors R are based on F, with F set to zero for negative F². The threshold expression of F² > σ(F²) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F² are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq	Occ. (<1)
Cl1	0.67199 (8)	0.75840 (5)	0.01612 (3)	0.05570 (19)
Cl2	0.2270 (3)	0.5061 (5)	0.02545 (13)	0.0676 (12)	0.653 (15)
Cl2'	0.2403 (3)	0.5502 (9)	0.0412 (4)	0.070 (3)	0.347 (15)
F1	0.9051 (2)	0.85834 (13)	0.05947 (11)	0.0915 (7)
F2	0.94983 (18)	0.73920 (13)	0.08421 (10)	0.0805 (6)
F3	0.89532 (17)	0.82357 (13)	0.15124 (9)	0.0722 (5)
F4	0.43674 (15)	0.43635 (10)	0.16241 (7)	0.0552 (4)
F5	0.50212 (16)	0.51978 (12)	0.09630 (9)	0.0693 (5)
F6	0.44470 (19)	0.40315 (14)	0.07147 (9)	0.0872 (7)
O1	0.64390 (15)	0.66486 (10)	0.22636 (7)	0.0378 (4)
O2	0.14813 (15)	0.59263 (9)	0.24189 (7)	0.0329 (3)
N1	0.45095 (19)	0.59688 (11)	0.25494 (8)	0.0291 (4)
N2	−0.05216 (19)	0.66161 (11)	0.25605 (8)	0.0283 (4)
C1	0.5205 (2)	0.64882 (12)	0.21976 (10)	0.0277 (4)
C2	0.4298 (2)	0.68560 (12)	0.17359 (9)	0.0264 (4)
H2	0.3594	0.6491	0.1558	0.032*
C3	0.3824 (2)	0.77078 (13)	0.17939 (9)	0.0304 (5)
C4	0.4844 (2)	0.74882 (13)	0.13117 (9)	0.0302 (5)
H4	0.4443	0.7468	0.0902	0.036*
C5	0.6308 (2)	0.77356 (13)	0.13406 (10)	0.0324 (5)
H5	0.6664	0.7866	0.1722	0.039*
C6	0.7173 (2)	0.77930 (14)	0.08877 (11)	0.0362 (5)
C7	0.8664 (3)	0.80168 (18)	0.09634 (14)	0.0542 (7)
C8	0.4284 (3)	0.81968 (14)	0.23245 (11)	0.0390 (5)
H8A	0.5227	0.8042	0.2440	0.059*
H8B	0.3649	0.8105	0.2658	0.059*
H8C	0.4274	0.8759	0.2218	0.059*
C9	0.2351 (2)	0.78755 (15)	0.15899 (11)	0.0387 (5)
H9A	0.2280	0.8427	0.1460	0.058*
H9B	0.1707	0.7783	0.1920	0.058*
H9C	0.2116	0.7524	0.1258	0.058*
C10	0.5010 (2)	0.55608 (12)	0.30557 (9)	0.0283 (4)
C11	0.4000 (2)	0.51516 (13)	0.33956 (10)	0.0322 (5)
H11	0.3058	0.5150	0.3270	0.039*
C12	0.4372 (3)	0.47600 (14)	0.39024 (10)	0.0358 (5)
H12	0.3683	0.4484	0.4123	0.043*
C13	0.5761 (3)	0.47564 (13)	0.41061 (10)	0.0343 (5)
C14	0.6182 (3)	0.43805 (14)	0.46424 (11)	0.0431 (6)
H14	0.5521	0.4097	0.4873	0.052*
C15	0.7531 (3)	0.44237 (15)	0.48295 (12)	0.0470 (6)
H15	0.7797	0.4176	0.5191	0.056*
C16	0.8524 (3)	0.48304 (15)	0.44914 (11)	0.0443 (6)
H16	0.9456	0.4859	0.4628	0.053*
C17	0.8165 (2)	0.51854 (14)	0.39682 (10)	0.0374 (5)
H17	0.8854	0.5449	0.3740	0.045*
C18	0.6773 (2)	0.51631 (13)	0.37624 (10)	0.0312 (4)
C19	0.6375 (2)	0.55512 (12)	0.32312 (9)	0.0299 (4)
H19	0.7058	0.5807	0.2994	0.036*
C20	0.0286 (2)	0.60868 (12)	0.22699 (9)	0.0254 (4)
C21	−0.0453 (2)	0.56913 (13)	0.17712 (9)	0.0277 (4)
H21	−0.1168	0.6026	0.1570	0.033*
C22	−0.0824 (2)	0.48145 (13)	0.18118 (9)	0.0289 (4)
C23	0.0254 (2)	0.50805 (13)	0.13649 (9)	0.0288 (4)
H23	−0.0081	0.5088	0.0944	0.035*
C24	0.1721 (2)	0.48659 (13)	0.14322 (9)	0.0298 (4)
H24	0.2022	0.4704	0.1816	0.036*
C25	0.2655 (2)	0.48783 (16)	0.10067 (10)	0.0391 (5)
C26	0.4110 (3)	0.46160 (17)	0.10780 (12)	0.0463 (6)
C27	−0.0401 (2)	0.43473 (14)	0.23534 (10)	0.0355 (5)
H27A	−0.1138	0.4377	0.2653	0.053*
H27B	0.0459	0.4568	0.2517	0.053*
H27C	−0.0249	0.3794	0.2241	0.053*
C28	−0.2230 (2)	0.45972 (15)	0.15708 (11)	0.0395 (5)
H28A	−0.2247	0.4032	0.1474	0.059*
H28B	−0.2418	0.4906	0.1211	0.059*
H28C	−0.2941	0.4711	0.1870	0.059*
C29	−0.0231 (2)	0.70345 (12)	0.30899 (10)	0.0282 (4)
C30	−0.1384 (2)	0.74173 (12)	0.33609 (10)	0.0333 (5)
H30	−0.2276	0.7384	0.3182	0.040*
C31	−0.1216 (3)	0.78325 (14)	0.38760 (11)	0.0384 (5)
H31	−0.1997	0.8083	0.4052	0.046*
C32	0.0095 (3)	0.78970 (14)	0.41532 (11)	0.0384 (5)
C33	0.0309 (3)	0.83374 (15)	0.46851 (12)	0.0491 (7)
H33	−0.0450	0.8605	0.4865	0.059*
C34	0.1589 (3)	0.83780 (15)	0.49368 (11)	0.0514 (7)
H34	0.1715	0.8671	0.5293	0.062*
C35	0.2722 (3)	0.79948 (15)	0.46779 (11)	0.0479 (7)
H35	0.3611	0.8032	0.4859	0.057*
C36	0.2568 (3)	0.75658 (14)	0.41665 (11)	0.0409 (6)
H36	0.3347	0.7305	0.3997	0.049*
C37	0.1248 (2)	0.75090 (13)	0.38880 (10)	0.0338 (5)
C38	0.1057 (2)	0.70761 (12)	0.33494 (10)	0.0312 (5)
H38	0.1824	0.6816	0.3170	0.037*
H2A	−0.132 (3)	0.6668 (13)	0.2440 (9)	0.022 (6)*
H1	0.365 (3)	0.5892 (15)	0.2472 (11)	0.039 (7)*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.0553 (4)	0.0665 (4)	0.0453 (3)	−0.0042 (3)	0.0152 (3)	−0.0084 (3)
Cl2	0.0340 (7)	0.136 (3)	0.0327 (7)	0.0050 (11)	0.0050 (5)	0.0149 (14)
Cl2'	0.0385 (13)	0.131 (6)	0.040 (3)	−0.0058 (19)	−0.0029 (12)	0.039 (3)
F1	0.0505 (11)	0.0977 (14)	0.1265 (18)	−0.0318 (11)	−0.0061 (12)	0.0623 (14)
F2	0.0335 (9)	0.0963 (15)	0.1117 (16)	0.0213 (10)	0.0170 (10)	0.0165 (13)
F3	0.0329 (9)	0.0979 (14)	0.0857 (13)	−0.0179 (9)	−0.0102 (9)	0.0028 (11)
F4	0.0276 (7)	0.0795 (11)	0.0584 (9)	0.0131 (7)	−0.0018 (7)	0.0173 (9)
F5	0.0238 (8)	0.0884 (13)	0.0956 (14)	−0.0049 (8)	0.0092 (8)	0.0256 (11)
F6	0.0486 (11)	0.1165 (17)	0.0963 (15)	0.0210 (11)	0.0111 (10)	−0.0522 (13)
O1	0.0180 (7)	0.0449 (9)	0.0506 (9)	−0.0053 (7)	−0.0075 (7)	0.0136 (8)
O2	0.0172 (7)	0.0385 (8)	0.0431 (9)	0.0025 (6)	−0.0058 (6)	−0.0056 (7)
N1	0.0168 (8)	0.0326 (9)	0.0380 (10)	−0.0030 (7)	−0.0057 (8)	0.0016 (8)
N2	0.0169 (8)	0.0321 (9)	0.0359 (10)	0.0001 (7)	−0.0042 (7)	−0.0027 (8)
C1	0.0196 (10)	0.0286 (10)	0.0351 (11)	0.0003 (8)	−0.0020 (8)	−0.0005 (9)
C2	0.0166 (9)	0.0311 (10)	0.0315 (11)	−0.0012 (8)	−0.0027 (8)	−0.0002 (8)
C3	0.0241 (10)	0.0331 (11)	0.0338 (11)	0.0020 (9)	−0.0005 (9)	0.0052 (9)
C4	0.0232 (10)	0.0389 (12)	0.0283 (10)	−0.0005 (9)	−0.0021 (8)	0.0029 (9)
C5	0.0251 (11)	0.0345 (11)	0.0375 (11)	0.0006 (9)	−0.0051 (9)	0.0047 (9)
C6	0.0268 (11)	0.0375 (12)	0.0443 (13)	0.0023 (9)	0.0036 (10)	0.0052 (10)
C7	0.0314 (14)	0.0605 (17)	0.0706 (19)	−0.0041 (13)	0.0048 (13)	0.0268 (15)
C8	0.0375 (13)	0.0362 (12)	0.0434 (13)	0.0041 (10)	0.0015 (10)	−0.0019 (10)
C9	0.0244 (11)	0.0462 (13)	0.0455 (13)	0.0066 (10)	0.0006 (10)	0.0105 (11)
C10	0.0256 (10)	0.0256 (10)	0.0336 (11)	−0.0017 (8)	−0.0030 (8)	0.0002 (8)
C11	0.0264 (10)	0.0332 (11)	0.0372 (11)	−0.0040 (9)	−0.0008 (9)	−0.0022 (9)
C12	0.0372 (13)	0.0338 (11)	0.0365 (12)	−0.0045 (10)	0.0023 (10)	−0.0004 (10)
C13	0.0405 (13)	0.0285 (10)	0.0337 (11)	0.0042 (10)	−0.0016 (10)	−0.0047 (9)
C14	0.0549 (16)	0.0376 (12)	0.0369 (12)	0.0071 (12)	−0.0002 (11)	−0.0007 (10)
C15	0.0618 (18)	0.0434 (14)	0.0359 (12)	0.0157 (13)	−0.0104 (12)	−0.0018 (11)
C16	0.0430 (14)	0.0435 (13)	0.0465 (13)	0.0150 (12)	−0.0140 (12)	−0.0067 (11)
C17	0.0328 (12)	0.0372 (11)	0.0421 (12)	0.0097 (10)	−0.0086 (10)	−0.0051 (10)
C18	0.0300 (11)	0.0275 (10)	0.0360 (11)	0.0062 (9)	−0.0050 (9)	−0.0051 (9)
C19	0.0233 (10)	0.0292 (10)	0.0372 (11)	0.0000 (8)	−0.0023 (9)	0.0001 (9)
C20	0.0193 (10)	0.0244 (9)	0.0324 (11)	−0.0038 (8)	−0.0019 (8)	0.0028 (8)
C21	0.0168 (9)	0.0337 (10)	0.0327 (11)	0.0026 (8)	−0.0031 (8)	0.0011 (9)
C22	0.0195 (10)	0.0333 (10)	0.0340 (11)	−0.0045 (8)	0.0011 (8)	−0.0026 (9)
C23	0.0203 (10)	0.0375 (11)	0.0288 (10)	−0.0013 (9)	−0.0019 (8)	−0.0043 (9)
C24	0.0228 (10)	0.0358 (11)	0.0309 (10)	−0.0016 (9)	−0.0019 (8)	−0.0010 (9)
C25	0.0253 (11)	0.0556 (15)	0.0365 (12)	0.0023 (11)	0.0034 (9)	0.0058 (11)
C26	0.0276 (12)	0.0649 (17)	0.0463 (14)	0.0038 (12)	0.0086 (11)	−0.0043 (13)
C27	0.0314 (12)	0.0349 (11)	0.0401 (12)	−0.0040 (10)	0.0051 (10)	0.0034 (10)
C28	0.0231 (11)	0.0473 (13)	0.0480 (13)	−0.0086 (10)	−0.0025 (10)	−0.0111 (11)
C29	0.0255 (10)	0.0261 (10)	0.0331 (11)	−0.0047 (8)	−0.0008 (9)	−0.0004 (8)
C30	0.0266 (11)	0.0290 (10)	0.0444 (12)	−0.0013 (9)	0.0028 (9)	−0.0007 (9)
C31	0.0342 (13)	0.0323 (11)	0.0488 (14)	−0.0008 (10)	0.0067 (11)	−0.0032 (10)
C32	0.0468 (14)	0.0323 (11)	0.0360 (12)	−0.0070 (10)	0.0018 (10)	−0.0020 (10)
C33	0.0654 (19)	0.0384 (13)	0.0434 (14)	−0.0113 (13)	0.0072 (13)	−0.0069 (11)
C34	0.075 (2)	0.0415 (14)	0.0380 (13)	−0.0180 (14)	−0.0051 (14)	−0.0040 (11)
C35	0.0603 (18)	0.0410 (13)	0.0422 (14)	−0.0143 (13)	−0.0188 (13)	0.0032 (11)
C36	0.0441 (14)	0.0369 (12)	0.0417 (12)	−0.0079 (11)	−0.0108 (11)	0.0018 (10)
C37	0.0379 (13)	0.0294 (11)	0.0342 (11)	−0.0051 (9)	−0.0049 (10)	0.0027 (9)
C38	0.0253 (10)	0.0304 (10)	0.0379 (12)	−0.0001 (8)	−0.0027 (9)	−0.0026 (9)

Geometric parameters (Å, º) top

Cl1—C6	1.727 (3)	C14—H14	0.9500
Cl2—Cl2'	0.836 (9)	C15—C16	1.402 (4)
Cl2—C25	1.759 (3)	C15—H15	0.9500
Cl2'—C25	1.721 (4)	C16—C17	1.365 (3)
F1—C7	1.321 (3)	C16—H16	0.9500
F2—C7	1.355 (3)	C17—C18	1.419 (3)
F3—C7	1.318 (4)	C17—H17	0.9500
F4—C26	1.324 (3)	C18—C19	1.416 (3)
F5—C26	1.344 (3)	C19—H19	0.9500
F6—C26	1.323 (3)	C20—C21	1.487 (3)
O1—C1	1.228 (2)	C21—C22	1.528 (3)
O2—C20	1.230 (2)	C21—C23	1.538 (3)
N1—C1	1.358 (3)	C21—H21	1.0000
N1—C10	1.416 (3)	C22—C28	1.504 (3)
N1—H1	0.86 (3)	C22—C27	1.508 (3)
N2—C20	1.354 (3)	C22—C23	1.513 (3)
N2—C29	1.413 (3)	C23—C24	1.467 (3)
N2—H2A	0.82 (2)	C23—H23	1.0000
C1—C2	1.492 (3)	C24—C25	1.313 (3)
C2—C3	1.517 (3)	C24—H24	0.9500
C2—C4	1.526 (3)	C25—C26	1.478 (3)
C2—H2	1.0000	C27—H27A	0.9800
C3—C4	1.509 (3)	C27—H27B	0.9800
C3—C8	1.518 (3)	C27—H27C	0.9800
C3—C9	1.518 (3)	C28—H28A	0.9800
C4—C5	1.472 (3)	C28—H28B	0.9800
C4—H4	1.0000	C28—H28C	0.9800
C5—C6	1.319 (3)	C29—C38	1.373 (3)
C5—H5	0.9500	C29—C30	1.422 (3)
C6—C7	1.495 (4)	C30—C31	1.364 (3)
C8—H8A	0.9800	C30—H30	0.9500
C8—H8B	0.9800	C31—C32	1.413 (4)
C8—H8C	0.9800	C31—H31	0.9500
C9—H9A	0.9800	C32—C37	1.421 (3)
C9—H9B	0.9800	C32—C33	1.424 (3)
C9—H9C	0.9800	C33—C34	1.359 (4)
C10—C19	1.373 (3)	C33—H33	0.9500
C10—C11	1.417 (3)	C34—C35	1.397 (4)
C11—C12	1.366 (3)	C34—H34	0.9500
C11—H11	0.9500	C35—C36	1.368 (3)
C12—C13	1.414 (3)	C35—H35	0.9500
C12—H12	0.9500	C36—C37	1.421 (3)
C13—C18	1.421 (3)	C36—H36	0.9500
C13—C14	1.422 (3)	C37—C38	1.427 (3)
C14—C15	1.368 (4)	C38—H38	0.9500

Cl2'—Cl2—C25	73.6 (3)	C10—C19—H19	119.8
Cl2—Cl2'—C25	78.6 (5)	C18—C19—H19	119.8
C1—N1—C10	128.00 (18)	O2—C20—N2	123.53 (19)
C1—N1—H1	117.1 (17)	O2—C20—C21	123.67 (19)
C10—N1—H1	114.8 (17)	N2—C20—C21	112.74 (17)
C20—N2—C29	128.63 (18)	C20—C21—C22	120.22 (18)
C20—N2—H2A	116.8 (15)	C20—C21—C23	122.55 (17)
C29—N2—H2A	114.2 (15)	C22—C21—C23	59.16 (14)
O1—C1—N1	123.3 (2)	C20—C21—H21	114.6
O1—C1—C2	123.93 (19)	C22—C21—H21	114.6
N1—C1—C2	112.73 (17)	C23—C21—H21	114.6
C1—C2—C3	120.80 (18)	C28—C22—C27	113.99 (19)
C1—C2—C4	121.70 (17)	C28—C22—C23	116.81 (18)
C3—C2—C4	59.48 (14)	C27—C22—C23	120.43 (18)
C1—C2—H2	114.6	C28—C22—C21	115.22 (19)
C3—C2—H2	114.6	C27—C22—C21	119.57 (18)
C4—C2—H2	114.6	C23—C22—C21	60.75 (14)
C4—C3—C2	60.57 (14)	C24—C23—C22	121.26 (19)
C4—C3—C8	120.59 (19)	C24—C23—C21	122.10 (18)
C2—C3—C8	119.82 (18)	C22—C23—C21	60.09 (13)
C4—C3—C9	115.91 (18)	C24—C23—H23	114.3
C2—C3—C9	115.64 (19)	C22—C23—H23	114.3
C8—C3—C9	114.12 (19)	C21—C23—H23	114.3
C5—C4—C3	121.43 (19)	C25—C24—C23	125.5 (2)
C5—C4—C2	120.08 (18)	C25—C24—H24	117.3
C3—C4—C2	59.95 (14)	C23—C24—H24	117.3
C5—C4—H4	114.8	C24—C25—C26	124.4 (2)
C3—C4—H4	114.8	C24—C25—Cl2'	118.7 (3)
C2—C4—H4	114.8	C26—C25—Cl2'	113.7 (2)
C6—C5—C4	126.3 (2)	C24—C25—Cl2	124.02 (19)
C6—C5—H5	116.9	C26—C25—Cl2	110.87 (18)
C4—C5—H5	116.9	Cl2'—C25—Cl2	27.8 (3)
C5—C6—C7	122.5 (2)	F6—C26—F4	106.6 (2)
C5—C6—Cl1	123.73 (19)	F6—C26—F5	105.5 (2)
C7—C6—Cl1	113.73 (19)	F4—C26—F5	107.0 (2)
F3—C7—F1	108.9 (3)	F6—C26—C25	113.0 (2)
F3—C7—F2	106.4 (2)	F4—C26—C25	112.0 (2)
F1—C7—F2	105.8 (2)	F5—C26—C25	112.3 (2)
F3—C7—C6	112.4 (2)	C22—C27—H27A	109.5
F1—C7—C6	112.5 (2)	C22—C27—H27B	109.5
F2—C7—C6	110.4 (3)	H27A—C27—H27B	109.5
C3—C8—H8A	109.5	C22—C27—H27C	109.5
C3—C8—H8B	109.5	H27A—C27—H27C	109.5
H8A—C8—H8B	109.5	H27B—C27—H27C	109.5
C3—C8—H8C	109.5	C22—C28—H28A	109.5
H8A—C8—H8C	109.5	C22—C28—H28B	109.5
H8B—C8—H8C	109.5	H28A—C28—H28B	109.5
C3—C9—H9A	109.5	C22—C28—H28C	109.5
C3—C9—H9B	109.5	H28A—C28—H28C	109.5
H9A—C9—H9B	109.5	H28B—C28—H28C	109.5
C3—C9—H9C	109.5	C38—C29—N2	124.2 (2)
H9A—C9—H9C	109.5	C38—C29—C30	120.0 (2)
H9B—C9—H9C	109.5	N2—C29—C30	115.76 (19)
C19—C10—N1	124.25 (19)	C31—C30—C29	120.4 (2)
C19—C10—C11	119.77 (19)	C31—C30—H30	119.8
N1—C10—C11	115.98 (19)	C29—C30—H30	119.8
C12—C11—C10	120.4 (2)	C30—C31—C32	121.4 (2)
C12—C11—H11	119.8	C30—C31—H31	119.3
C10—C11—H11	119.8	C32—C31—H31	119.3
C11—C12—C13	121.4 (2)	C31—C32—C37	118.5 (2)
C11—C12—H12	119.3	C31—C32—C33	122.7 (3)
C13—C12—H12	119.3	C37—C32—C33	118.8 (2)
C12—C13—C18	118.1 (2)	C34—C33—C32	120.5 (3)
C12—C13—C14	123.1 (2)	C34—C33—H33	119.7
C18—C13—C14	118.8 (2)	C32—C33—H33	119.7
C15—C14—C13	120.5 (3)	C33—C34—C35	120.8 (2)
C15—C14—H14	119.7	C33—C34—H34	119.6
C13—C14—H14	119.7	C35—C34—H34	119.6
C14—C15—C16	120.5 (2)	C36—C35—C34	120.8 (3)
C14—C15—H15	119.8	C36—C35—H35	119.6
C16—C15—H15	119.8	C34—C35—H35	119.6
C17—C16—C15	120.7 (2)	C35—C36—C37	120.2 (3)
C17—C16—H16	119.7	C35—C36—H36	119.9
C15—C16—H16	119.7	C37—C36—H36	119.9
C16—C17—C18	120.6 (2)	C32—C37—C36	118.9 (2)
C16—C17—H17	119.7	C32—C37—C38	119.5 (2)
C18—C17—H17	119.7	C36—C37—C38	121.6 (2)
C19—C18—C17	121.2 (2)	C29—C38—C37	120.2 (2)
C19—C18—C13	119.8 (2)	C29—C38—H38	119.9
C17—C18—C13	118.9 (2)	C37—C38—H38	119.9
C10—C19—C18	120.5 (2)

C10—N1—C1—O1	3.6 (4)	O2—C20—C21—C23	−4.4 (3)
C10—N1—C1—C2	−174.8 (2)	N2—C20—C21—C23	178.52 (18)
O1—C1—C2—C3	−72.5 (3)	C20—C21—C22—C28	139.9 (2)
N1—C1—C2—C3	106.0 (2)	C23—C21—C22—C28	−107.9 (2)
O1—C1—C2—C4	−1.6 (3)	C20—C21—C22—C27	−1.7 (3)
N1—C1—C2—C4	176.88 (19)	C23—C21—C22—C27	110.5 (2)
C1—C2—C3—C4	111.0 (2)	C20—C21—C22—C23	−112.2 (2)
C1—C2—C3—C8	0.5 (3)	C28—C22—C23—C24	−143.1 (2)
C4—C2—C3—C8	−110.5 (2)	C27—C22—C23—C24	2.5 (3)
C1—C2—C3—C9	−142.4 (2)	C21—C22—C23—C24	111.6 (2)
C4—C2—C3—C9	106.6 (2)	C28—C22—C23—C21	105.3 (2)
C2—C3—C4—C5	−109.0 (2)	C27—C22—C23—C21	−109.1 (2)
C8—C3—C4—C5	0.3 (3)	C20—C21—C23—C24	−1.9 (3)
C9—C3—C4—C5	144.9 (2)	C22—C21—C23—C24	−110.2 (2)
C8—C3—C4—C2	109.3 (2)	C20—C21—C23—C22	108.3 (2)
C9—C3—C4—C2	−106.2 (2)	C22—C23—C24—C25	160.7 (2)
C1—C2—C4—C5	1.6 (3)	C21—C23—C24—C25	−127.2 (3)
C3—C2—C4—C5	111.2 (2)	C23—C24—C25—C26	−176.4 (2)
C1—C2—C4—C3	−109.5 (2)	C23—C24—C25—Cl2'	25.3 (7)
C3—C4—C5—C6	−158.2 (2)	C23—C24—C25—Cl2	−6.8 (5)
C2—C4—C5—C6	130.7 (2)	Cl2—Cl2'—C25—C24	−109.3 (6)
C4—C5—C6—C7	−177.3 (2)	Cl2—Cl2'—C25—C26	90.1 (4)
C4—C5—C6—Cl1	0.2 (4)	Cl2'—Cl2—C25—C24	87.8 (6)
C5—C6—C7—F3	−7.5 (4)	Cl2'—Cl2—C25—C26	−101.4 (4)
Cl1—C6—C7—F3	174.77 (19)	C24—C25—C26—F6	120.5 (3)
C5—C6—C7—F1	−130.9 (3)	Cl2'—C25—C26—F6	−80.2 (7)
Cl1—C6—C7—F1	51.3 (3)	Cl2—C25—C26—F6	−50.2 (4)
C5—C6—C7—F2	111.1 (3)	C24—C25—C26—F4	0.1 (4)
Cl1—C6—C7—F2	−66.6 (3)	Cl2'—C25—C26—F4	159.4 (7)
C1—N1—C10—C19	−8.9 (4)	Cl2—C25—C26—F4	−170.7 (4)
C1—N1—C10—C11	170.2 (2)	C24—C25—C26—F5	−120.3 (3)
C19—C10—C11—C12	1.2 (3)	Cl2'—C25—C26—F5	39.0 (7)
N1—C10—C11—C12	−178.0 (2)	Cl2—C25—C26—F5	68.9 (4)
C10—C11—C12—C13	0.6 (3)	C20—N2—C29—C38	12.2 (3)
C11—C12—C13—C18	−1.0 (3)	C20—N2—C29—C30	−166.7 (2)
C11—C12—C13—C14	177.7 (2)	C38—C29—C30—C31	0.6 (3)
C12—C13—C14—C15	−177.3 (2)	N2—C29—C30—C31	179.5 (2)
C18—C13—C14—C15	1.3 (3)	C29—C30—C31—C32	0.2 (3)
C13—C14—C15—C16	−0.8 (4)	C30—C31—C32—C37	−0.8 (4)
C14—C15—C16—C17	−0.5 (4)	C30—C31—C32—C33	178.9 (2)
C15—C16—C17—C18	1.3 (4)	C31—C32—C33—C34	179.6 (2)
C16—C17—C18—C19	177.8 (2)	C37—C32—C33—C34	−0.7 (4)
C16—C17—C18—C13	−0.8 (3)	C32—C33—C34—C35	0.5 (4)
C12—C13—C18—C19	−0.4 (3)	C33—C34—C35—C36	−0.4 (4)
C14—C13—C18—C19	−179.1 (2)	C34—C35—C36—C37	0.5 (4)
C12—C13—C18—C17	178.2 (2)	C31—C32—C37—C36	−179.5 (2)
C14—C13—C18—C17	−0.5 (3)	C33—C32—C37—C36	0.8 (3)
N1—C10—C19—C18	176.51 (19)	C31—C32—C37—C38	0.8 (3)
C11—C10—C19—C18	−2.6 (3)	C33—C32—C37—C38	−179.0 (2)
C17—C18—C19—C10	−176.4 (2)	C35—C36—C37—C32	−0.7 (3)
C13—C18—C19—C10	2.2 (3)	C35—C36—C37—C38	179.0 (2)
C29—N2—C20—O2	−4.7 (3)	N2—C29—C38—C37	−179.50 (19)
C29—N2—C20—C21	172.35 (19)	C30—C29—C38—C37	−0.6 (3)
O2—C20—C21—C22	66.2 (3)	C32—C37—C38—C29	−0.1 (3)
N2—C20—C21—C22	−110.9 (2)	C36—C37—C38—C29	−179.8 (2)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···O2	0.86 (3)	2.09 (3)	2.932 (2)	167 (2)
N2—H2A···O1ⁱ	0.82 (2)	2.19 (3)	3.003 (2)	169 (2)

Symmetry code: (i) x−1, y, z.

Experimental details

Crystal data
Chemical formula	C₁₉H₁₇ClF₃NO
M_r	367.79
Crystal system, space group	Orthorhombic, P2₁2₁2₁
Temperature (K)	113
a, b, c (Å)	9.6310 (8), 16.9090 (16), 22.485 (2)
V (Å³)	3661.6 (6)
Z	8
Radiation type	Mo Kα
µ (mm⁻¹)	0.24
Crystal size (mm)	0.32 × 0.22 × 0.14

Data collection
Diffractometer	Rigaku Saturn diffractometer
Absorption correction	Multi-scan (CrystalClear; Rigaku/MSC, 2005)
T_min, T_max	0.926, 0.967
No. of measured, independent and observed [I > 2σ(I)] reflections	34375, 8701, 8283
R_int	0.046
(sin θ/λ)_max (Å⁻¹)	0.658

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.053, 0.115, 1.14
No. of reflections	8701
No. of parameters	473
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.23, −0.28
Absolute structure	Flack (1983), with how many Friedel pairs?
Absolute structure parameter	−0.05 (6)

Computer programs: CrystalClear (Rigaku/MSC, 2005), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Bruker, 1997), CrystalStructure (Rigaku/MSC, 2005).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···O2	0.86 (3)	2.09 (3)	2.932 (2)	167 (2)
N2—H2A···O1ⁱ	0.82 (2)	2.19 (3)	3.003 (2)	169 (2)

Symmetry code: (i) x−1, y, z.

Acknowledgements

This work was supported by the National Natural Science Foundation of China (grant No. 20376059) and Tianjin Polytechnic University

References

Bruker (1997). SADABS. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
Flack, H. D. (1983). Acta Cryst. A39, 876–881. CrossRef CAS Web of Science IUCr Journals Google Scholar
Liu, D.-Q. & Yan, F.-Y. (2007). Acta Cryst. E63, o4202. Web of Science CSD CrossRef IUCr Journals Google Scholar
Punja, N. (1981). Eur. Patent EP 0031199. Google Scholar
Rigaku/MSC (2005). CrystalClear and CrystalStructure. Rigaku/MSC, The Woodlands, Texas, USA. Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar

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Volume 64| Part 11| November 2008| Page o2191

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organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

(E)-3-(2-Chloro-3,3,3-tri­fluoro­prop-1-en­yl)-2,2-di­methyl-N-(2-naphth­yl)cyclo­propane­carboxamide

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Experimental

Crystal data

Data collection

Refinement

Supporting information

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organic compounds

(E)-3-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl-N-(2-naphthyl)cyclopropanecarboxamide