Home Physical Sciences Crystal structure of 2-benzoyl-3-(4-methoxyphenyl)cyclopropane-1,1-dicarbonitrile, C19H14N2O2
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Crystal structure of 2-benzoyl-3-(4-methoxyphenyl)cyclopropane-1,1-dicarbonitrile, C19H14N2O2

  • Changming You and Changqing Wang EMAIL logo
Published/Copyright: September 16, 2017

Abstract

C19H14N2O2, monoclinic C2/c (no. 15), a = 19.8907(8) Å, b = 12.0860(5) Å, c = 15.5260(7) Å, β = 120.588(1)°, V = 3213.06(20) Å3, Z = 8, Rgt(F) = 0.0504, wRref(F2) = 0.1426, T = 296 K.

CCDC no.:: 1568605

The crystal structure is shown in the f igure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1

Data collection and handling.

Crystal:Colorless block
Size:0.22 × 0.20 × 0.18 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.08 mm−1
Dif fractometer, scan mode:Bruker APEXII, ω
θmax28.6°
N(hkl)measured, N(hkl)unique, Rint:13416, 4055, 0.030
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 2291
N(param)ref ined:253
Programs:SHELX [4], DIAMOND [5], BRUKER [6]
Table 2

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

AtomxyzUiso*/Ueq
C10.12536(16)0.46622(17)0.13246(17)0.0817(6)
C20.0798(2)0.5313(2)0.1555(2)0.1070(9)
C30.0119(3)0.4929(3)0.1426(3)0.1237(13)
C4−0.0117(2)0.3895(3)0.1082(3)0.1339(13)
C50.03325(14)0.32125(19)0.0857(2)0.0872(7)
C60.10155(10)0.35982(13)0.09677(12)0.0559(4)
C70.14958(10)0.29359(13)0.06900(14)0.0603(4)
C80.13583(10)0.17085(13)0.05529(13)0.0543(4)
C90.19223(9)0.10020(13)0.04533(12)0.0516(4)
C100.11153(9)0.12321(12)−0.04863(13)0.0524(4)
C110.10767(11)0.19373(15)−0.12574(15)0.0672(5)
C120.05336(10)0.03694(14)−0.08464(13)0.0592(4)
C130.21478(9)−0.01325(13)0.08595(12)0.0503(4)
C140.17542(11)−0.07426(14)0.12244(14)0.0625(5)
C150.19799(12)−0.18060(16)0.15694(16)0.0700(5)
C160.26002(10)−0.22877(14)0.15505(14)0.0628(4)
C170.30008(11)−0.16970(16)0.12021(15)0.0685(5)
C180.27735(10)−0.06263(16)0.08619(14)0.0623(5)
C190.33745(14)−0.39023(19)0.18261(18)0.0970(7)
H19A0.3252−0.38850.11430.146*
H19B0.3408−0.46570.20380.146*
H19C0.3866−0.35400.22420.146*
H10.1737(16)0.485(2)0.140(2)0.123(10)*
H20.0933(18)0.610(3)0.178(3)0.168(12)*
H3−0.0172(19)0.540(2)0.160(2)0.154(11)*
H4−0.061(2)0.355(3)0.088(3)0.174(13)*
H50.0155(12)0.2539(17)0.0579(16)0.081(6)*
H60.1090(9)0.1384(12)0.0842(11)0.051(4)*
H70.2308(9)0.1426(13)0.0423(12)0.057(4)*
H80.1320(11)−0.0418(14)0.1267(14)0.071(5)*
H90.1698(12)−0.2197(17)0.1826(16)0.090(6)*
H100.3045(11)−0.0213(15)0.0617(15)0.077(6)*
H110.3446(13)−0.2021(16)0.1176(16)0.094(7)*
N10.10417(13)0.24665(18)−0.18834(18)0.1087(7)
N20.00791(10)−0.03160(14)−0.11037(14)0.0850(5)
O10.19882(9)0.33535(10)0.05534(14)0.0966(5)
O20.27790(9)−0.33477(11)0.19075(12)0.0872(4)

Source of material

A mixture of phenacyl bromide (0.238 g, 1.2 mmol), triphenylarsine (0.167 g, 0.15 mmol), 2-(4-methoxybenzylidene)malononitrile (1 mmol), and NaHCO3 (0.240 g, 3 mmol) was stirred in CH3CN at room temperature. Completion of the reaction was monitored by TLC using hexane/ethyl acetate (6:1). The solution was f iltered on a pad of Celite and washed with ethyl acetate (5 mL) followed by dichloromethane (5 mL). The f iltrate was concentrated under reduced pressure to af ford the crude product, which was purif ied by column chromatography using hexane/ethyl acetate and silica gel as the stationary phase. The pure product was a white solid (0.25 g, yield 86%). Colourless crystals suitable for X-ray dif fraction were obtained by slow evaporation of the title compound in a mixture of dichloromethane with hexane at room temperature.

Experimental details

All non-hydrogen atoms were ref ined anisotropically. The hydrogen atoms were located by geometrical calculations, and their positions and thermal parameters were f ixed during the structure ref inement.

Discussion

The synthesis and application of multisubstituted cyclopropanes have been subjects of great interest because of the roles as basic structural elements in a wide range of biologically active compounds and important intermediates in organic synthesis [1], [2], [3]. We have been interested in this type of derivatives and reported several crystallographic analyses of the products. As a continuation of our work, the multisubstituted cyclopropane derivative 2-benzoyl-3-(4-methoxyphenyl)cyclopropane-1,1-dicarbonitrile was synthesized from 2-(4-methoxybenzylidene)malononitrile and the corresponding phenacyl bromide.

There is one complete molecule in the asymmetric unit (cf. the f igure). The C8—C10, and C9—C10 bond lengths are 1.541(2), 1.549(2) Å, respectively. The C8—C9 bond length is 1.479(2), slightly shorter than the other two C—C bonds in the cyclopropanyl moiety. The bond angles of C9—C8—C10, C8—C9—C10 and C8—C10—C9 are 61.66(11)°, 61.13(11)° and 57.2(1)°, respectively. Thus angles of ca. 60° are present. The benzoyl and aryl groups are situated in an anti conf iguration at the cyclopropane ring.

Acknowledgement

The authors thank the Natural Science Foundation of China (no. 21662019) for f inancial support.

References

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Received: 2017-4-19
Accepted: 2017-8-12
Published Online: 2017-9-16
Published in Print: 2017-11-27

©2017 Changming You et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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