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

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890

(2SR,3RS)-Benz­yl[4-chloro-1-(4-chloro­phen­yl)-1-meth­oxy­carbon­yl-2-but­yl]­ammonium chloride

aDepartment of Chemistry, University of Oslo, PO Box 1033 Blindern, N-0315 Oslo, Norway
*Correspondence e-mail: c.h.gorbitz@kjemi.uio.no

(Received 22 September 2008; accepted 24 September 2008; online 27 September 2008)

In the racemic hydro­chloride salt of the title ester, C19H22Cl2NO2+·Cl, the penta­noic acid chain shows a mixture of trans and gauche orientations to give an overall helical conformation. The dihedral angle between the two aromatic rings is 26.11 (10)°. The charged secondary amine function participates in two N—H⋯Cl hydrogen bonds.

Related literature

For a related structure, see: Froimowitz et al. (1998[Froimowitz, M., Wu, K.-M., George, C., VanDerveer, D., Shi, Q. & Deutsch, H. M. (1998). Struct. Chem. 9, 295-303.]).

[Scheme 1]

Experimental

Crystal data
  • C19H22Cl2NO2+·Cl

  • Mr = 402.73

  • Triclinic, [P \overline 1]

  • a = 9.263 (2) Å

  • b = 10.432 (3) Å

  • c = 11.490 (3) Å

  • α = 115.954 (3)°

  • β = 93.925 (3)°

  • γ = 103.015 (3)°

  • V = 954.8 (4) Å3

  • Z = 2

  • Mo Kα radiation

  • μ = 0.49 mm−1

  • T = 296 (2) K

  • 0.60 × 0.38 × 0.18 mm

Data collection
  • Bruker APEX II CCD diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996[Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.]) Tmin = 0.782, Tmax = 0.915

  • 8767 measured reflections

  • 4422 independent reflections

  • 3320 reflections with I > 2σ(I)

  • Rint = 0.024

Refinement
  • R[F2 > 2σ(F2)] = 0.046

  • wR(F2) = 0.159

  • S = 1.03

  • 4422 reflections

  • 227 parameters

  • H-atom parameters constrained

  • Δρmax = 0.43 e Å−3

  • Δρmin = −0.36 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
N1—H2⋯Cl3 0.90 2.28 3.0890 (18) 150
N1—H1⋯Cl3i 0.90 2.59 3.2447 (18) 131
Symmetry code: (i) -x, -y+1, -z.

Data collection: APEX2 (Bruker, 2007[Bruker (2007). APEX2 and SAINT-Plus. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT-Plus (Bruker, 2007[Bruker (2007). APEX2 and SAINT-Plus. Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT-Plus; program(s) used to solve structure: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL.

Supporting information


Comment top

The title molecule, (I), is a β-amino acid ester resulting from a rhodium-catalyzed C—H insertion reaction between methyl-(4-chlorophenyl)diazo acetate and Boc-protected N-benzyl-3-chloropropanamine. Full details will be published elsewhere.

Related literature top

For a related structure, see: Froimowitz et al. (1998).

Experimental top

Colourless blocks of (I) were grown by diffusion of diethylether into 100 µl of a solution containing about 5 mg of the title compound in methanol.

Refinement top

The H atoms were positioned with idealized geometry (N–H = 0.90 Å, C–H = 0.93-0.98 Å) and refined as riding with Uiso(H) = 1.2Ueq(C, N) or 1.5Ueq(methyl C).

Computing details top

Data collection: SMART (Bruker, 2001); cell refinement: SAINT-Plus (Bruker, 2001); data reduction: SAINT-Plus (Bruker, 2001); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. : The molecular structure of (I). Displacement ellipsoids are shown at the 50% probability level and H-atoms are shown as spheres of arbitrary size.
[Figure 2] Fig. 2. : Molecular packing and unit cell of (I) viewed along the a axis. Hydrogen bonding is indicated by dashed lines, H-atoms bonded to C have been omitted for clarity.
(2SR,3RS)-Benzyl[4-chloro-1-(4-chlorophenyl)-1-methoxycarbonyl- 2-butyl]ammonium chloride top
Crystal data top
C19H22Cl2NO2+·ClZ = 2
Mr = 402.73F(000) = 420
Triclinic, P1Dx = 1.401 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 9.263 (2) ÅCell parameters from 3509 reflections
b = 10.432 (3) Åθ = 2.0–28.7°
c = 11.490 (3) ŵ = 0.49 mm1
α = 115.954 (3)°T = 296 K
β = 93.925 (3)°Block, colourless
γ = 103.015 (3)°0.60 × 0.38 × 0.18 mm
V = 954.8 (4) Å3
Data collection top
Bruker APEXII CCD
diffractometer
4422 independent reflections
Radiation source: fine-focus sealed tube3320 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.024
Detector resolution: 8.3 pixels mm-1θmax = 28.7°, θmin = 2.0°
sets of exposures each taken over 0.5° ω rotation scansh = 1210
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
k = 1312
Tmin = 0.782, Tmax = 0.915l = 1515
8767 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.047Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.159H-atom parameters constrained
S = 1.04 w = 1/[σ2(Fo2) + (0.097P)2 + 0.1562P]
where P = (Fo2 + 2Fc2)/3
4422 reflections(Δ/σ)max = 0.002
227 parametersΔρmax = 0.44 e Å3
0 restraintsΔρmin = 0.36 e Å3
Crystal data top
C19H22Cl2NO2+·Clγ = 103.015 (3)°
Mr = 402.73V = 954.8 (4) Å3
Triclinic, P1Z = 2
a = 9.263 (2) ÅMo Kα radiation
b = 10.432 (3) ŵ = 0.49 mm1
c = 11.490 (3) ÅT = 296 K
α = 115.954 (3)°0.60 × 0.38 × 0.18 mm
β = 93.925 (3)°
Data collection top
Bruker APEXII CCD
diffractometer
4422 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
3320 reflections with I > 2σ(I)
Tmin = 0.782, Tmax = 0.915Rint = 0.024
8767 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0470 restraints
wR(F2) = 0.159H-atom parameters constrained
S = 1.04Δρmax = 0.44 e Å3
4422 reflectionsΔρmin = 0.36 e Å3
227 parameters
Special details top

Experimental. Crystal grew over 48 h.

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. Data were collected by measuring three sets of exposures with the detector set at 2θ = 29°, crystal-to-detector distance 6.00 cm. Refinement of F2 against ALL reflections.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Cl10.64470 (8)0.98821 (8)0.38456 (7)0.0691 (2)
Cl20.26825 (11)0.01534 (7)0.06864 (6)0.0787 (3)
Cl30.17315 (6)0.47020 (7)0.12520 (5)0.05352 (19)
O10.11480 (18)0.6582 (2)0.40412 (15)0.0512 (4)
O20.28993 (18)0.62358 (19)0.52192 (14)0.0473 (4)
N10.18786 (18)0.67376 (17)0.17013 (15)0.0330 (3)
H10.11420.65050.21070.040*
H20.18380.59030.09660.040*
C10.2347 (2)0.6371 (2)0.41927 (17)0.0346 (4)
C20.3435 (2)0.6218 (2)0.32432 (17)0.0321 (4)
H210.44520.65830.37730.039*
C30.3372 (2)0.7230 (2)0.25943 (17)0.0314 (4)
H310.34970.82370.32990.038*
C40.4634 (2)0.7305 (2)0.18192 (19)0.0377 (4)
H410.45710.63020.11660.045*
H420.44640.78520.13490.045*
C50.6210 (2)0.8022 (3)0.2633 (2)0.0457 (5)
H510.69300.80140.20580.055*
H520.64180.74460.30640.055*
C60.3211 (2)0.4594 (2)0.22692 (18)0.0338 (4)
C70.4464 (2)0.4091 (3)0.1945 (2)0.0431 (5)
H710.54250.47440.23440.052*
C80.4308 (3)0.2642 (3)0.1046 (2)0.0507 (6)
H810.51540.23150.08330.061*
C90.2888 (3)0.1685 (2)0.0466 (2)0.0495 (6)
C100.1623 (3)0.2137 (3)0.0776 (2)0.0494 (5)
H1010.06680.14690.03800.059*
C110.1778 (2)0.3591 (2)0.1681 (2)0.0423 (5)
H1110.09250.39030.18990.051*
C120.1968 (3)0.6398 (3)0.6215 (2)0.0590 (7)
H1210.25420.64800.69840.088*
H1220.11000.55450.58720.088*
H1230.16460.72780.64450.088*
C130.1553 (3)0.7857 (2)0.1302 (2)0.0416 (5)
H1310.22400.79830.07350.050*
H1320.05350.74610.07900.050*
C140.1697 (2)0.9353 (2)0.2434 (2)0.0387 (4)
C150.0533 (3)0.9580 (3)0.3120 (3)0.0589 (6)
H1510.03190.87910.29070.071*
C160.0627 (4)1.0968 (3)0.4118 (3)0.0726 (8)
H1610.01561.11040.45830.087*
C170.1861 (4)1.2151 (3)0.4434 (3)0.0646 (7)
H1710.19061.30890.50970.077*
C180.3036 (3)1.1941 (3)0.3761 (2)0.0562 (6)
H1810.38831.27360.39740.067*
C190.2947 (3)1.0547 (3)0.2771 (2)0.0456 (5)
H1910.37421.04080.23220.055*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Cl10.0507 (4)0.0516 (4)0.0684 (4)0.0046 (3)0.0023 (3)0.0063 (3)
Cl20.1402 (8)0.0425 (4)0.0514 (4)0.0395 (4)0.0239 (4)0.0128 (3)
Cl30.0418 (3)0.0546 (4)0.0430 (3)0.0064 (2)0.0086 (2)0.0077 (2)
O10.0410 (9)0.0740 (12)0.0479 (8)0.0263 (8)0.0165 (7)0.0306 (8)
O20.0516 (9)0.0586 (10)0.0389 (7)0.0191 (8)0.0122 (6)0.0269 (7)
N10.0316 (8)0.0309 (8)0.0339 (7)0.0081 (6)0.0027 (6)0.0138 (6)
C10.0379 (10)0.0281 (9)0.0313 (9)0.0053 (8)0.0045 (7)0.0103 (7)
C20.0278 (9)0.0334 (10)0.0332 (8)0.0074 (7)0.0039 (7)0.0149 (7)
C30.0289 (9)0.0284 (9)0.0306 (8)0.0048 (7)0.0015 (7)0.0106 (7)
C40.0349 (10)0.0377 (11)0.0375 (9)0.0058 (8)0.0077 (8)0.0170 (8)
C50.0351 (11)0.0457 (12)0.0527 (12)0.0067 (9)0.0097 (9)0.0220 (10)
C60.0390 (10)0.0330 (10)0.0340 (9)0.0136 (8)0.0097 (7)0.0176 (8)
C70.0411 (11)0.0451 (12)0.0520 (11)0.0188 (9)0.0169 (9)0.0261 (10)
C80.0627 (15)0.0514 (14)0.0564 (13)0.0329 (12)0.0298 (11)0.0307 (11)
C90.0855 (18)0.0354 (11)0.0353 (10)0.0277 (12)0.0167 (11)0.0175 (9)
C100.0565 (14)0.0359 (11)0.0491 (12)0.0099 (10)0.0034 (10)0.0175 (10)
C110.0390 (11)0.0360 (11)0.0491 (11)0.0110 (9)0.0030 (9)0.0180 (9)
C120.0731 (17)0.0678 (17)0.0396 (11)0.0207 (14)0.0212 (11)0.0263 (12)
C130.0464 (12)0.0381 (11)0.0405 (10)0.0126 (9)0.0013 (8)0.0194 (9)
C140.0373 (11)0.0360 (11)0.0447 (10)0.0133 (8)0.0010 (8)0.0201 (9)
C150.0377 (12)0.0492 (14)0.0818 (17)0.0139 (10)0.0119 (11)0.0227 (13)
C160.0671 (19)0.0614 (18)0.087 (2)0.0355 (15)0.0280 (16)0.0221 (15)
C170.083 (2)0.0421 (14)0.0609 (15)0.0286 (14)0.0017 (14)0.0136 (12)
C180.0662 (16)0.0382 (12)0.0588 (14)0.0058 (11)0.0061 (12)0.0246 (11)
C190.0476 (12)0.0427 (12)0.0502 (11)0.0100 (9)0.0065 (9)0.0267 (10)
Geometric parameters (Å, º) top
Cl1—C51.776 (2)C8—C91.370 (4)
Cl2—C91.745 (2)C8—H810.9300
O1—C11.196 (3)C9—C101.372 (3)
O2—C11.330 (2)C10—C111.379 (3)
O2—C121.454 (3)C10—H1010.9300
N1—C31.502 (2)C11—H1110.9300
N1—C131.508 (3)C12—H1210.9600
N1—H10.9000C12—H1220.9600
N1—H20.9000C12—H1230.9600
C1—C21.517 (3)C13—C141.501 (3)
C2—C61.522 (3)C13—H1310.9700
C2—C31.544 (3)C13—H1320.9700
C2—H210.9800C14—C151.381 (3)
C3—C41.526 (3)C14—C191.381 (3)
C3—H310.9800C15—C161.376 (4)
C4—C51.508 (3)C15—H1510.9300
C4—H410.9700C16—C171.370 (4)
C4—H420.9700C16—H1610.9300
C5—H510.9700C17—C181.380 (4)
C5—H520.9700C17—H1710.9300
C6—C71.387 (3)C18—C191.379 (3)
C6—C111.395 (3)C18—H1810.9300
C7—C81.374 (3)C19—H1910.9300
C7—H710.9300
C1—O2—C12116.08 (18)C9—C8—H81120.4
C3—N1—C13115.50 (15)C7—C8—H81120.4
C3—N1—H1108.4C8—C9—C10121.5 (2)
C13—N1—H1108.4C8—C9—Cl2119.32 (19)
C3—N1—H2108.4C10—C9—Cl2119.2 (2)
C13—N1—H2108.4C9—C10—C11119.5 (2)
H1—N1—H2107.5C9—C10—H101120.3
O1—C1—O2124.21 (18)C11—C10—H101120.3
O1—C1—C2124.68 (17)C10—C11—C6120.2 (2)
O2—C1—C2111.11 (17)C10—C11—H111119.9
C1—C2—C6111.18 (15)C6—C11—H111119.9
C1—C2—C3111.11 (15)O2—C12—H121109.5
C6—C2—C3114.25 (14)O2—C12—H122109.5
C1—C2—H21106.6H121—C12—H122109.5
C6—C2—H21106.6O2—C12—H123109.5
C3—C2—H21106.6H121—C12—H123109.5
N1—C3—C4109.14 (15)H122—C12—H123109.5
N1—C3—C2111.71 (14)C14—C13—N1114.43 (16)
C4—C3—C2112.34 (16)C14—C13—H131108.7
N1—C3—H31107.8N1—C13—H131108.7
C4—C3—H31107.8C14—C13—H132108.7
C2—C3—H31107.8N1—C13—H132108.7
C5—C4—C3115.28 (16)H131—C13—H132107.6
C5—C4—H41108.5C15—C14—C19118.5 (2)
C3—C4—H41108.5C15—C14—C13120.1 (2)
C5—C4—H42108.5C19—C14—C13121.3 (2)
C3—C4—H42108.5C16—C15—C14120.4 (2)
H41—C4—H42107.5C16—C15—H151119.8
C4—C5—Cl1111.82 (16)C14—C15—H151119.8
C4—C5—H51109.3C17—C16—C15120.8 (3)
Cl1—C5—H51109.3C17—C16—H161119.6
C4—C5—H52109.3C15—C16—H161119.6
Cl1—C5—H52109.3C16—C17—C18119.6 (2)
H51—C5—H52107.9C16—C17—H171120.2
C7—C6—C11118.70 (19)C18—C17—H171120.2
C7—C6—C2119.31 (18)C19—C18—C17119.6 (2)
C11—C6—C2121.99 (17)C19—C18—H181120.2
C8—C7—C6121.0 (2)C17—C18—H181120.2
C8—C7—H71119.5C18—C19—C14121.2 (2)
C6—C7—H71119.5C18—C19—H191119.4
C9—C8—C7119.1 (2)C14—C19—H191119.4
C1—C2—C3—C4170.19 (15)C3—C2—C6—C1184.9 (2)
C2—C3—C4—C565.1 (2)C11—C6—C7—C81.2 (3)
C3—C4—C5—Cl159.2 (2)C2—C6—C7—C8178.37 (18)
C3—C2—C1—O2145.64 (16)C6—C7—C8—C90.2 (3)
C2—C1—O2—C12178.60 (18)C7—C8—C9—C100.8 (3)
C1—C2—C6—C7138.62 (18)C7—C8—C9—Cl2179.55 (17)
C2—C3—N1—C13164.81 (16)C8—C9—C10—C110.7 (3)
C3—N1—C13—C1453.8 (2)Cl2—C9—C10—C11179.63 (16)
N1—C13—C14—C1580.7 (3)C9—C10—C11—C60.3 (3)
C12—O2—C1—O11.5 (3)C7—C6—C11—C101.3 (3)
O1—C1—C2—C693.9 (2)C2—C6—C11—C10178.28 (18)
O2—C1—C2—C685.91 (19)N1—C13—C14—C19102.7 (2)
O1—C1—C2—C334.5 (3)C19—C14—C15—C160.1 (4)
C13—N1—C3—C470.3 (2)C13—C14—C15—C16176.8 (2)
C1—C2—C3—N166.78 (18)C14—C15—C16—C171.1 (5)
C6—C2—C3—N160.0 (2)C15—C16—C17—C181.4 (5)
C6—C2—C3—C463.0 (2)C16—C17—C18—C190.7 (4)
N1—C3—C4—C5170.40 (17)C17—C18—C19—C140.3 (3)
C3—C2—C6—C794.6 (2)C15—C14—C19—C180.6 (3)
C1—C2—C6—C1141.8 (2)C13—C14—C19—C18176.10 (19)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H2···Cl30.902.283.0890 (18)150
N1—H1···Cl3i0.902.593.2447 (18)131
Symmetry code: (i) x, y+1, z.

Experimental details

Crystal data
Chemical formulaC19H22Cl2NO2+·Cl
Mr402.73
Crystal system, space groupTriclinic, P1
Temperature (K)296
a, b, c (Å)9.263 (2), 10.432 (3), 11.490 (3)
α, β, γ (°)115.954 (3), 93.925 (3), 103.015 (3)
V3)954.8 (4)
Z2
Radiation typeMo Kα
µ (mm1)0.49
Crystal size (mm)0.60 × 0.38 × 0.18
Data collection
DiffractometerBruker APEXII CCD
diffractometer
Absorption correctionMulti-scan
(SADABS; Sheldrick, 1996)
Tmin, Tmax0.782, 0.915
No. of measured, independent and
observed [I > 2σ(I)] reflections
8767, 4422, 3320
Rint0.024
(sin θ/λ)max1)0.675
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.047, 0.159, 1.04
No. of reflections4422
No. of parameters227
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.44, 0.36

Computer programs: SMART (Bruker, 2001), SAINT-Plus (Bruker, 2001), SHELXTL (Sheldrick, 2008).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H2···Cl30.902.283.0890 (18)150
N1—H1···Cl3i0.902.593.2447 (18)131
Symmetry code: (i) x, y+1, z.
 

References

First citationBruker (2007). APEX2 and SAINT-Plus. Bruker AXS Inc., Madison, Wisconsin, USA.  Google Scholar
First citationFroimowitz, M., Wu, K.-M., George, C., VanDerveer, D., Shi, Q. & Deutsch, H. M. (1998). Struct. Chem. 9, 295–303.  Web of Science CSD CrossRef CAS Google Scholar
First citationSheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.  Google Scholar
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Follow Acta Cryst. E
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds