n-Undeca­nyl 2-(4-chloro­anilino)-4,4-dimethyl-6-oxocyclo­hex-1-ene­carbo­dithio­ate

El Ashry, E.S.H.; Amer, M.R.; Shah, M.R.; Ng, S.W.

doi:10.1107/S1600536809006163

organic compounds

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ISSN: 2056-9890

Volume 65| Part 3| March 2009| Page o599

doi:10.1107/S1600536809006163

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n-Undecanyl 2-(4-chloroanilino)-4,4-dimethyl-6-oxocyclohex-1-enecarbodithioate

El Sayed H. El Ashry,^a Mohammed R. Amer,^a M. Raza Shah ^a and Seik Weng Ng ^b ^*

^aH.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan, and ^bDepartment of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia
^*Correspondence e-mail: seikweng@um.edu.my

(Received 19 February 2009; accepted 19 February 2009; online 25 February 2009)

The six-membered cyclohexene ring in the title compound, C₂₆H₃₈ClNOS₂, adopts an envelope conformation, with the C atom bearing the two methyl groups representing the flap. This atom deviates by 0.642 (4) Å from the plane passing through the other five atoms of the ring (r.m.s. deviation = 0.053 Å). The molecular conformation is stabilized by an intramolecular N—H⋯S hydrogen bond.

Related literature

For background, see: El Ashry et al. (2009 ).

Experimental

Crystal data

C₂₆H₃₈ClNOS₂
M_r = 480.14
Triclinic, $[P \overline 1]$
a = 7.9865 (2) Å
b = 11.8015 (4) Å
c = 14.9676 (4) Å
α = 97.522 (2)°
β = 94.004 (3)°
γ = 106.134 (2)°
V = 1335.13 (7) Å³
Z = 2
Mo Kα radiation
μ = 0.32 mm⁻¹
T = 100 K
0.20 × 0.15 × 0.10 mm

Data collection

Bruker SMART APEX diffractometer
Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ) T_min = 0.892, T_max = 0.969
12760 measured reflections
6108 independent reflections
3899 reflections with I > 2σ(I)
R_int = 0.051

Refinement

R[F² > 2σ(F²)] = 0.052
wR(F²) = 0.157
S = 1.01
6108 reflections
287 parameters
1 restraint
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.33 e Å⁻³
Δρ_min = −0.36 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1⋯S2	0.89 (1)	2.10 (2)	2.873 (2)	146 (3)

Data collection: APEX2 (Bruker, 2008 ); cell refinement: SAINT (Bruker, 2008); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: X-SEED (Barbour, 2001 ); software used to prepare material for publication: publCIF (Westrip, 2009 ).

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809006163/bt2878sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536809006163/bt2878Isup2.hkl

checkCIF report

Related literature top

For background, see: El Ashry et al. (2009).

Experimental top

To a solution of (4-chlorophenylamino)-5,5-dimethyl-cyclohex-2-en-1-one (0.1 mol) in DMSO (20 ml) and sodium hydroxide (0.4 g) in water (1 ml), carbon disulfphide (0.3 mol) was added in the course of 30 minutes. The mixture was stirred for 20 min below 283 K, and then 1-bromoundecane (0.1 mol) was added dropwise at room temperature for 30 min. The reaction mixture was left for 24 h and then diluted with water (200 ml) and acidified with 10% hydrochloric acid. The resulting precipitate was collected by filtration, dried and purified on silica gel column (40% ethyl acetate in hexane) to give yellow crystals (48% yield; mp 368 K).

Computing details top

Data collection: APEX2 (Bruker, 2008); cell refinement: SAINT (Bruker, 2008); data reduction: SAINT (Bruker, 2008); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: X-SEED (Barbour, 2001); software used to prepare material for publication: publCIF (Westrip, 2009).

Figures top

Fig. 1. Anisotropic displacement ellipsoid plot (Barbour, 2001) plot of C₂₆H₃₈ClNOS₂ at the 70% probability level; hydrogen atoms are drawn as spheres of arbitrary radius.

n-Undecanyl 2-(4-chloroanilino)-4,4-dimethyl-6-oxocyclohex-1-enecarbodithioate top

Crystal data top

C₂₆H₃₈ClNOS₂	Z = 2
M_r = 480.14	F(000) = 516
Triclinic, P1	D_x = 1.194 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 7.9865 (2) Å	Cell parameters from 1537 reflections
b = 11.8015 (4) Å	θ = 2.5–22.0°
c = 14.9676 (4) Å	µ = 0.32 mm⁻¹
α = 97.522 (2)°	T = 100 K
β = 94.004 (3)°	Irregular block, yellow
γ = 106.134 (2)°	0.20 × 0.15 × 0.10 mm
V = 1335.13 (7) Å³

Data collection top

Bruker SMART APEX diffractometer	6108 independent reflections
Radiation source: fine-focus sealed tube	3899 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.051
ω scans	θ_max = 27.5°, θ_min = 1.4°
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)	h = −10→10
T_min = 0.892, T_max = 0.969	k = −15→15
12760 measured reflections	l = −19→19

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.052	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.157	H atoms treated by a mixture of independent and constrained refinement
S = 1.01	w = 1/[σ²(F_o²) + (0.074P)²] where P = (F_o² + 2F_c²)/3
6108 reflections	(Δ/σ)_max = 0.001
287 parameters	Δρ_max = 0.33 e Å⁻³
1 restraint	Δρ_min = −0.36 e Å⁻³

Crystal data top

C₂₆H₃₈ClNOS₂	γ = 106.134 (2)°
M_r = 480.14	V = 1335.13 (7) Å³
Triclinic, P1	Z = 2
a = 7.9865 (2) Å	Mo Kα radiation
b = 11.8015 (4) Å	µ = 0.32 mm⁻¹
c = 14.9676 (4) Å	T = 100 K
α = 97.522 (2)°	0.20 × 0.15 × 0.10 mm
β = 94.004 (3)°

Data collection top

Bruker SMART APEX diffractometer	6108 independent reflections
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)	3899 reflections with I > 2σ(I)
T_min = 0.892, T_max = 0.969	R_int = 0.051
12760 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.052	1 restraint
wR(F²) = 0.157	H atoms treated by a mixture of independent and constrained refinement
S = 1.01	Δρ_max = 0.33 e Å⁻³
6108 reflections	Δρ_min = −0.36 e Å⁻³
287 parameters

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

	x	y	z	U_iso*/U_eq
Cl1	0.19825 (13)	0.41121 (9)	1.03994 (6)	0.0563 (3)
S1	0.63724 (9)	0.24958 (6)	0.39696 (5)	0.02316 (18)
S2	0.39872 (10)	0.15853 (6)	0.52890 (5)	0.0290 (2)
N1	0.4552 (3)	0.3457 (2)	0.68108 (16)	0.0254 (5)
H1	0.416 (4)	0.2718 (14)	0.651 (2)	0.050 (11)*
O1	0.7692 (3)	0.47573 (16)	0.43665 (13)	0.0286 (5)
C1	0.7341 (3)	0.4897 (2)	0.51557 (18)	0.0212 (6)
C2	0.8197 (4)	0.6096 (2)	0.57245 (18)	0.0244 (6)
H2A	0.7635	0.6678	0.5514	0.029*
H2B	0.9444	0.6354	0.5613	0.029*
C3	0.8122 (3)	0.6156 (2)	0.67421 (18)	0.0230 (6)
C4	0.6254 (3)	0.5507 (2)	0.68855 (18)	0.0221 (6)
H4A	0.6187	0.5495	0.7542	0.027*
H4B	0.5464	0.5960	0.6681	0.027*
C5	0.5613 (3)	0.4250 (2)	0.63920 (18)	0.0230 (6)
C6	0.6116 (3)	0.3932 (2)	0.55220 (18)	0.0218 (6)
C7	0.9411 (4)	0.5570 (3)	0.71535 (19)	0.0300 (7)
H7A	1.0607	0.5995	0.7053	0.045*
H7B	0.9125	0.4734	0.6865	0.045*
H7C	0.9329	0.5603	0.7806	0.045*
C8	0.8553 (4)	0.7455 (3)	0.7191 (2)	0.0335 (7)
H8A	0.7681	0.7812	0.6950	0.050*
H8B	0.9721	0.7897	0.7063	0.050*
H8C	0.8532	0.7491	0.7847	0.050*
C9	0.5498 (3)	0.2748 (2)	0.49969 (18)	0.0228 (6)
C10	0.5423 (4)	0.0905 (2)	0.36058 (19)	0.0275 (6)
H10A	0.5528	0.0470	0.4120	0.033*
H10B	0.4163	0.0727	0.3390	0.033*
C11	0.6397 (4)	0.0507 (3)	0.28414 (18)	0.0278 (6)
H11A	0.5910	−0.0368	0.2659	0.033*
H11B	0.7645	0.0673	0.3077	0.033*
C12	0.6303 (4)	0.1104 (3)	0.20027 (19)	0.0297 (7)
H12A	0.5057	0.0963	0.1776	0.036*
H12B	0.6836	0.1976	0.2176	0.036*
C13	0.7230 (4)	0.0651 (3)	0.12447 (19)	0.0297 (7)
H13A	0.6651	−0.0213	0.1047	0.036*
H13B	0.8458	0.0746	0.1482	0.036*
C14	0.7234 (4)	0.1293 (3)	0.04282 (19)	0.0319 (7)
H14A	0.6006	0.1169	0.0176	0.038*
H14B	0.7767	0.2160	0.0632	0.038*
C15	0.8222 (4)	0.0882 (3)	−0.03191 (19)	0.0334 (7)
H15A	0.7756	0.0004	−0.0489	0.040*
H15B	0.9474	0.1070	−0.0084	0.040*
C16	0.8086 (4)	0.1459 (3)	−0.11602 (19)	0.0305 (7)
H16A	0.8572	0.2336	−0.0990	0.037*
H16B	0.6832	0.1285	−0.1386	0.037*
C17	0.9041 (4)	0.1038 (3)	−0.19232 (19)	0.0312 (7)
H17A	1.0307	0.1254	−0.1709	0.037*
H17B	0.8603	0.0156	−0.2069	0.037*
C18	0.8816 (4)	0.1564 (3)	−0.27808 (19)	0.0294 (7)
H18A	0.9328	0.2442	−0.2644	0.035*
H18B	0.7547	0.1396	−0.2972	0.035*
C19	0.9668 (4)	0.1080 (3)	−0.35609 (19)	0.0323 (7)
H19A	1.0946	0.1280	−0.3383	0.039*
H19B	0.9193	0.0198	−0.3683	0.039*
C20	0.9360 (5)	0.1577 (3)	−0.4419 (2)	0.0421 (8)
H20A	0.9942	0.1245	−0.4899	0.063*
H20B	0.9841	0.2449	−0.4305	0.063*
H20C	0.8098	0.1360	−0.4610	0.063*
C21	0.3962 (4)	0.3664 (3)	0.76804 (19)	0.0264 (6)
C22	0.2856 (4)	0.4365 (3)	0.7835 (2)	0.0357 (8)
H22	0.2508	0.4750	0.7366	0.043*
C23	0.2256 (4)	0.4507 (3)	0.8673 (2)	0.0420 (8)
H23	0.1499	0.4992	0.8783	0.050*
C24	0.2753 (4)	0.3946 (3)	0.9345 (2)	0.0347 (7)
C25	0.3846 (5)	0.3240 (3)	0.9201 (2)	0.0427 (8)
H25	0.4186	0.2856	0.9673	0.051*
C26	0.4448 (4)	0.3095 (3)	0.8357 (2)	0.0375 (8)
H26	0.5196	0.2603	0.8246	0.045*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.0583 (6)	0.0751 (7)	0.0282 (4)	0.0072 (5)	0.0165 (4)	0.0020 (4)
S1	0.0251 (4)	0.0190 (4)	0.0240 (4)	0.0041 (3)	0.0038 (3)	0.0034 (3)
S2	0.0293 (4)	0.0188 (4)	0.0367 (4)	0.0013 (3)	0.0120 (3)	0.0042 (3)
N1	0.0269 (13)	0.0211 (13)	0.0272 (13)	0.0033 (10)	0.0097 (10)	0.0046 (11)
O1	0.0343 (12)	0.0214 (10)	0.0270 (11)	0.0011 (8)	0.0093 (9)	0.0049 (8)
C1	0.0183 (14)	0.0177 (13)	0.0273 (15)	0.0042 (11)	0.0019 (11)	0.0047 (11)
C2	0.0249 (15)	0.0189 (14)	0.0279 (15)	0.0030 (11)	0.0029 (12)	0.0057 (12)
C3	0.0183 (14)	0.0236 (14)	0.0250 (14)	0.0032 (11)	0.0022 (11)	0.0029 (12)
C4	0.0216 (14)	0.0201 (14)	0.0246 (14)	0.0058 (11)	0.0032 (11)	0.0032 (11)
C5	0.0196 (14)	0.0222 (14)	0.0283 (15)	0.0070 (11)	−0.0006 (11)	0.0073 (12)
C6	0.0198 (14)	0.0220 (14)	0.0235 (14)	0.0059 (11)	0.0011 (11)	0.0047 (11)
C7	0.0241 (15)	0.0379 (18)	0.0269 (15)	0.0068 (13)	0.0003 (12)	0.0074 (13)
C8	0.0330 (17)	0.0254 (16)	0.0369 (17)	0.0019 (13)	0.0055 (14)	0.0002 (13)
C9	0.0191 (14)	0.0242 (14)	0.0277 (15)	0.0091 (11)	0.0026 (11)	0.0065 (12)
C10	0.0314 (16)	0.0199 (15)	0.0272 (15)	0.0008 (12)	0.0024 (12)	0.0041 (12)
C11	0.0332 (17)	0.0244 (15)	0.0253 (15)	0.0097 (12)	0.0011 (12)	0.0004 (12)
C12	0.0337 (17)	0.0267 (16)	0.0270 (16)	0.0070 (13)	0.0015 (13)	0.0031 (12)
C13	0.0298 (16)	0.0285 (16)	0.0271 (16)	0.0060 (13)	−0.0014 (12)	−0.0013 (13)
C14	0.0371 (18)	0.0296 (16)	0.0280 (16)	0.0092 (13)	0.0035 (13)	0.0024 (13)
C15	0.0361 (18)	0.0376 (18)	0.0279 (16)	0.0133 (14)	0.0041 (14)	0.0039 (14)
C16	0.0324 (17)	0.0280 (16)	0.0305 (16)	0.0094 (13)	0.0029 (13)	0.0017 (13)
C17	0.0295 (17)	0.0364 (18)	0.0276 (16)	0.0101 (13)	0.0026 (13)	0.0043 (13)
C18	0.0297 (16)	0.0261 (16)	0.0322 (16)	0.0072 (13)	0.0042 (13)	0.0058 (13)
C19	0.0274 (16)	0.0376 (18)	0.0333 (17)	0.0079 (13)	0.0072 (13)	0.0117 (14)
C20	0.044 (2)	0.051 (2)	0.0373 (19)	0.0168 (17)	0.0141 (16)	0.0157 (16)
C21	0.0242 (15)	0.0273 (16)	0.0250 (15)	0.0036 (12)	0.0038 (12)	0.0029 (12)
C22	0.0321 (17)	0.053 (2)	0.0291 (16)	0.0205 (15)	0.0067 (13)	0.0119 (15)
C23	0.0337 (18)	0.065 (2)	0.0345 (18)	0.0235 (17)	0.0114 (14)	0.0077 (17)
C24	0.0323 (17)	0.0421 (19)	0.0229 (15)	0.0004 (14)	0.0097 (13)	0.0004 (14)
C25	0.060 (2)	0.040 (2)	0.0296 (17)	0.0152 (17)	0.0037 (16)	0.0102 (15)
C26	0.049 (2)	0.0312 (18)	0.0371 (18)	0.0181 (15)	0.0081 (15)	0.0079 (14)

Geometric parameters (Å, º) top

Cl1—C24	1.740 (3)	C12—H12B	0.9900
S1—C9	1.757 (3)	C13—C14	1.520 (4)
S1—C10	1.811 (3)	C13—H13A	0.9900
S2—C9	1.685 (3)	C13—H13B	0.9900
N1—C5	1.332 (3)	C14—C15	1.517 (4)
N1—C21	1.429 (3)	C14—H14A	0.9900
N1—H1	0.885 (10)	C14—H14B	0.9900
O1—C1	1.234 (3)	C15—C16	1.519 (4)
C1—C6	1.474 (4)	C15—H15A	0.9900
C1—C2	1.504 (4)	C15—H15B	0.9900
C2—C3	1.522 (4)	C16—C17	1.522 (4)
C2—H2A	0.9900	C16—H16A	0.9900
C2—H2B	0.9900	C16—H16B	0.9900
C3—C4	1.520 (4)	C17—C18	1.518 (4)
C3—C8	1.525 (4)	C17—H17A	0.9900
C3—C7	1.529 (4)	C17—H17B	0.9900
C4—C5	1.499 (4)	C18—C19	1.519 (4)
C4—H4A	0.9900	C18—H18A	0.9900
C4—H4B	0.9900	C18—H18B	0.9900
C5—C6	1.423 (4)	C19—C20	1.514 (4)
C6—C9	1.446 (4)	C19—H19A	0.9900
C7—H7A	0.9800	C19—H19B	0.9900
C7—H7B	0.9800	C20—H20A	0.9800
C7—H7C	0.9800	C20—H20B	0.9800
C8—H8A	0.9800	C20—H20C	0.9800
C8—H8B	0.9800	C21—C26	1.376 (4)
C8—H8C	0.9800	C21—C22	1.380 (4)
C10—C11	1.524 (4)	C22—C23	1.380 (4)
C10—H10A	0.9900	C22—H22	0.9500
C10—H10B	0.9900	C23—C24	1.368 (4)
C11—C12	1.525 (4)	C23—H23	0.9500
C11—H11A	0.9900	C24—C25	1.373 (5)
C11—H11B	0.9900	C25—C26	1.390 (4)
C12—C13	1.516 (4)	C25—H25	0.9500
C12—H12A	0.9900	C26—H26	0.9500

C9—S1—C10	102.95 (13)	C12—C13—H13A	108.9
C5—N1—C21	127.5 (2)	C14—C13—H13A	108.9
C5—N1—H1	116 (2)	C12—C13—H13B	108.9
C21—N1—H1	116 (2)	C14—C13—H13B	108.9
O1—C1—C6	121.4 (2)	H13A—C13—H13B	107.7
O1—C1—C2	117.2 (2)	C15—C14—C13	114.0 (3)
C6—C1—C2	121.4 (2)	C15—C14—H14A	108.8
C1—C2—C3	116.1 (2)	C13—C14—H14A	108.8
C1—C2—H2A	108.3	C15—C14—H14B	108.8
C3—C2—H2A	108.3	C13—C14—H14B	108.8
C1—C2—H2B	108.3	H14A—C14—H14B	107.7
C3—C2—H2B	108.3	C14—C15—C16	113.2 (3)
H2A—C2—H2B	107.4	C14—C15—H15A	108.9
C4—C3—C2	107.3 (2)	C16—C15—H15A	108.9
C4—C3—C8	108.7 (2)	C14—C15—H15B	108.9
C2—C3—C8	109.7 (2)	C16—C15—H15B	108.9
C4—C3—C7	110.5 (2)	H15A—C15—H15B	107.7
C2—C3—C7	110.7 (2)	C15—C16—C17	113.9 (2)
C8—C3—C7	109.9 (2)	C15—C16—H16A	108.8
C5—C4—C3	113.6 (2)	C17—C16—H16A	108.8
C5—C4—H4A	108.8	C15—C16—H16B	108.8
C3—C4—H4A	108.8	C17—C16—H16B	108.8
C5—C4—H4B	108.8	H16A—C16—H16B	107.7
C3—C4—H4B	108.8	C18—C17—C16	113.7 (2)
H4A—C4—H4B	107.7	C18—C17—H17A	108.8
N1—C5—C6	122.3 (3)	C16—C17—H17A	108.8
N1—C5—C4	116.4 (2)	C18—C17—H17B	108.8
C6—C5—C4	121.3 (2)	C16—C17—H17B	108.8
C5—C6—C9	124.1 (2)	H17A—C17—H17B	107.7
C5—C6—C1	116.2 (2)	C17—C18—C19	113.5 (2)
C9—C6—C1	119.7 (2)	C17—C18—H18A	108.9
C3—C7—H7A	109.5	C19—C18—H18A	108.9
C3—C7—H7B	109.5	C17—C18—H18B	108.9
H7A—C7—H7B	109.5	C19—C18—H18B	108.9
C3—C7—H7C	109.5	H18A—C18—H18B	107.7
H7A—C7—H7C	109.5	C20—C19—C18	112.5 (3)
H7B—C7—H7C	109.5	C20—C19—H19A	109.1
C3—C8—H8A	109.5	C18—C19—H19A	109.1
C3—C8—H8B	109.5	C20—C19—H19B	109.1
H8A—C8—H8B	109.5	C18—C19—H19B	109.1
C3—C8—H8C	109.5	H19A—C19—H19B	107.8
H8A—C8—H8C	109.5	C19—C20—H20A	109.5
H8B—C8—H8C	109.5	C19—C20—H20B	109.5
C6—C9—S2	125.1 (2)	H20A—C20—H20B	109.5
C6—C9—S1	117.8 (2)	C19—C20—H20C	109.5
S2—C9—S1	117.15 (16)	H20A—C20—H20C	109.5
C11—C10—S1	108.50 (19)	H20B—C20—H20C	109.5
C11—C10—H10A	110.0	C26—C21—C22	120.1 (3)
S1—C10—H10A	110.0	C26—C21—N1	118.4 (3)
C11—C10—H10B	110.0	C22—C21—N1	121.4 (3)
S1—C10—H10B	110.0	C23—C22—C21	119.8 (3)
H10A—C10—H10B	108.4	C23—C22—H22	120.1
C10—C11—C12	114.8 (2)	C21—C22—H22	120.1
C10—C11—H11A	108.6	C24—C23—C22	119.9 (3)
C12—C11—H11A	108.6	C24—C23—H23	120.1
C10—C11—H11B	108.6	C22—C23—H23	120.1
C12—C11—H11B	108.6	C23—C24—C25	121.1 (3)
H11A—C11—H11B	107.5	C23—C24—Cl1	120.0 (3)
C13—C12—C11	113.2 (2)	C25—C24—Cl1	119.0 (3)
C13—C12—H12A	108.9	C24—C25—C26	119.1 (3)
C11—C12—H12A	108.9	C24—C25—H25	120.4
C13—C12—H12B	108.9	C26—C25—H25	120.4
C11—C12—H12B	108.9	C21—C26—C25	120.0 (3)
H12A—C12—H12B	107.7	C21—C26—H26	120.0
C12—C13—C14	113.5 (2)	C25—C26—H26	120.0

O1—C1—C2—C3	−165.2 (2)	C10—S1—C9—C6	174.7 (2)
C6—C1—C2—C3	15.6 (4)	C10—S1—C9—S2	−5.8 (2)
C1—C2—C3—C4	−45.9 (3)	C9—S1—C10—C11	−166.72 (19)
C1—C2—C3—C8	−163.9 (2)	S1—C10—C11—C12	−60.6 (3)
C1—C2—C3—C7	74.7 (3)	C10—C11—C12—C13	−177.9 (2)
C2—C3—C4—C5	55.4 (3)	C11—C12—C13—C14	−176.6 (3)
C8—C3—C4—C5	174.0 (2)	C12—C13—C14—C15	177.6 (3)
C7—C3—C4—C5	−65.3 (3)	C13—C14—C15—C16	175.3 (3)
C21—N1—C5—C6	179.8 (3)	C14—C15—C16—C17	−178.9 (3)
C21—N1—C5—C4	−0.5 (4)	C15—C16—C17—C18	176.8 (3)
C3—C4—C5—N1	144.5 (2)	C16—C17—C18—C19	−176.1 (2)
C3—C4—C5—C6	−35.7 (3)	C17—C18—C19—C20	177.6 (3)
N1—C5—C6—C9	2.0 (4)	C5—N1—C21—C26	−116.3 (3)
C4—C5—C6—C9	−177.8 (2)	C5—N1—C21—C22	67.0 (4)
N1—C5—C6—C1	−178.1 (2)	C26—C21—C22—C23	0.8 (5)
C4—C5—C6—C1	2.1 (4)	N1—C21—C22—C23	177.4 (3)
O1—C1—C6—C5	−171.1 (2)	C21—C22—C23—C24	−0.3 (5)
C2—C1—C6—C5	8.2 (4)	C22—C23—C24—C25	0.0 (5)
O1—C1—C6—C9	8.8 (4)	C22—C23—C24—Cl1	−179.4 (3)
C2—C1—C6—C9	−172.0 (2)	C23—C24—C25—C26	−0.1 (5)
C5—C6—C9—S2	4.6 (4)	Cl1—C24—C25—C26	179.3 (3)
C1—C6—C9—S2	−175.2 (2)	C22—C21—C26—C25	−0.9 (5)
C5—C6—C9—S1	−175.8 (2)	N1—C21—C26—C25	−177.6 (3)
C1—C6—C9—S1	4.3 (3)	C24—C25—C26—C21	0.6 (5)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···S2	0.89 (1)	2.10 (2)	2.873 (2)	146 (3)

Experimental details

Crystal data
Chemical formula	C₂₆H₃₈ClNOS₂
M_r	480.14
Crystal system, space group	Triclinic, P1
Temperature (K)	100
a, b, c (Å)	7.9865 (2), 11.8015 (4), 14.9676 (4)
α, β, γ (°)	97.522 (2), 94.004 (3), 106.134 (2)
V (Å³)	1335.13 (7)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.32
Crystal size (mm)	0.20 × 0.15 × 0.10

Data collection
Diffractometer	Bruker SMART APEX diffractometer
Absorption correction	Multi-scan (SADABS; Sheldrick, 1996)
T_min, T_max	0.892, 0.969
No. of measured, independent and observed [I > 2σ(I)] reflections	12760, 6108, 3899
R_int	0.051
(sin θ/λ)_max (Å⁻¹)	0.650

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.052, 0.157, 1.01
No. of reflections	6108
No. of parameters	287
No. of restraints	1
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.33, −0.36

Computer programs: APEX2 (Bruker, 2008), SAINT (Bruker, 2008), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), X-SEED (Barbour, 2001), publCIF (Westrip, 2009).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···S2	0.89 (1)	2.10 (2)	2.873 (2)	146 (3)

Acknowledgements

We thank the Higher Education Commission of Pakistan and the University of Malaya for supporting this study.

References

Barbour, L. J. (2001). J. Supramol. Chem. 1, 189–191. CrossRef CAS Google Scholar
Bruker (2008). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
El Ashry, E. S. H., Amer, M. R., Raza Shah, M. & Ng, S. W. (2009). Acta Cryst. E65, o597. Web of Science CSD CrossRef IUCr Journals Google Scholar
Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany. Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Westrip, S. P. (2009). publCIF. In preparation. Google Scholar

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Volume 65| Part 3| March 2009| Page o599

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

n-Undeca­nyl 2-(4-chloro­anilino)-4,4-di­methyl-6-oxo­cyclo­hex-1-ene­carbo­di­thio­ate

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Experimental

Crystal data

Data collection

Refinement

Supporting information

Acknowledgements

References

organic compounds

n-Undecanyl 2-(4-chloroanilino)-4,4-dimethyl-6-oxocyclohex-1-enecarbodithioate