Home Crystal structure of 1,1-dimethyl-3-(2-phenylethyl)urea, C11H16N2O
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Crystal structure of 1,1-dimethyl-3-(2-phenylethyl)urea, C11H16N2O

  • Gamal A. El-Hiti EMAIL logo , Keith Smith , Mohammed B. Alshammari , Mohammad Hayal Alotaibi and Benson M. Kariuki
Published/Copyright: May 21, 2016

Abstract

C11H16N2O, orthorhombic, Pbca (no. 61), a = 10.7388(6) Å, b = 9.8449(5) Å, c = 21.1259(14) Å, V = 2233.5(2) Å3, Z = 8, Rgt(F) = 0.0582, wRref(F2) = 0.1795, T = 293 K.

CCDC no.:: 1478571

Tables 1 and 2 contain details of the measurement method and a list of the atoms including atomic coordinates and displacement parameters.

Table 1

Data collection and handling.

Crystal:Colourless, block Size 0.37 × 0.17 × 0.10 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.8 cm−1
Diffractometer, scan mode:SuperNova, ω
2θmax, completeness:59.4°, >99%
N(hkl)measured, N(hkl)unique, Rint:7627, 2680, 0.025
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 1669
N(param)refined:129
Programs:SHELX [13], CrysAlisPRO [14], WinGX [15]
Table 2

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

AtomxyzUiso*/Ueq
C10.48541(18)0.06211(19)0.35228(8)0.0580(5)
C20.5322(2)0.1652(2)0.31509(11)0.0743(6)
H20.60150.21350.32880.089*
C30.4777(3)0.1979(3)0.25766(12)0.0921(8)
H30.51070.26780.23330.111*
C40.3765(3)0.1288(3)0.23680(13)0.0993(8)
H40.34090.15050.19800.119*
C50.3273(2)0.0284(3)0.27259(13)0.0975(8)
H50.2573−0.01830.25860.117*
C60.3810(2)−0.0053(2)0.33001(11)0.0784(6)
H60.3463−0.07460.35420.094*
C70.54501(19)0.0256(2)0.41422(9)0.0687(6)
H7A0.4881−0.03060.43840.082*
H7B0.55990.10800.43820.082*
C80.66752(18)−0.04998(19)0.40590(9)0.0618(5)
H8A0.6514−0.13470.38390.074*
H8B0.72220.00410.37940.074*
C90.79739(16)0.01667(16)0.49494(10)0.0565(5)
C100.8638(2)−0.1564(2)0.57266(11)0.0833(7)
H10A0.7839−0.18220.58910.125*
H10B0.9248−0.16120.60580.125*
H10C0.8868−0.21700.53900.125*
C110.9276(2)0.0821(2)0.58375(12)0.0848(7)
H11A0.93580.16290.55870.127*
H11B1.00880.04700.59340.127*
H11C0.88460.10310.62240.127*
N10.73091(15)−0.07966(14)0.46471(7)0.0604(4)
H10.7261−0.15990.48060.072*
N20.85761(15)−0.01881(16)0.54863(8)0.0675(5)
O10.80282(14)0.13384(12)0.47359(8)0.0751(5)

Source of material

1,1-Dimethyl-3-(2-phenylethyl)urea was synthesized from reaction of (2-phenylethyl)amine with dimethylcarbamoyl chloride (1.1 mole equivalents) in the presence of triethylamine (1.4 mole equivalents) in dichloromethane under reflux for 1 h. Recrystallization using a mixture of ethyl acetate and diethyl ether (1:3 by volume) gave the title compound (~99%) as colourless crystals, mp 89–90 °C (lit. 88–90 °C [1]; 81–82 °C [2]).

Experimental details

All H atoms were placed in calculated positions and refined using a riding model. For the methyl groups, C—H bonds were fixed at 0.96 Å and Uiso(H) set to 1.5 Ueq(C) with free rotation around the C—C bond (HFIX 137 in SHELX [13]). For the rest of the hydrogens, Uiso(H) was set to 1.2 Ueq(C) with aromatic C—H and N—H distances of 0.93 and 0.86 Å, respectively.

Discussion

The synthesis of substituted ureas is of great interest for both academia and industry since ureas represent various biologically active compounds [2], [3], [4]. Urea derivatives can be synthesized using various efficient procedures [5], [6], [7]. Regioselective lithiation of aromatic ureas with lithium reagents followed by reaction with electrophiles at low temperatures is considered to be one of the most clean, efficient and convenient processes for the production of a large number of substituted derivatives in high yields [8], [9], [10], [11].

The asymetric unit (Figure) of the crystal structure consists of a molecule of C11H16N2O. In the crystal, the amide group is involved in N—H⋯O hydrogen bonding (N⋯O distance = 2.850(2) Å, N—H⋯O angle = 152.4°) leading to the formation of C(4) chains [12] along the [010] direction.

Acknowledgements:

The authors extend their appreciation to the College of Applied Medical Sciences Research Centre and the Deanship of Scientific Research at King Saud University for their funding of this research.

References

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Received: 2016-3-14
Accepted: 2016-5-8
Published Online: 2016-5-21
Published in Print: 2016-12-1

©2016 Gamal A. El-Hiti et al., published by De Gruyter.

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

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  73. Crystal structure of 4-(4-((3-bromophenyl)amino)-6-(tert-butyl)-3-(2-hydroxypropan-2-yl)cinnolin-8-yl)-2-methylbut-3-yn-2-ol, C26H30BrN3O2
  74. Crystal structure poly-(μ2-1-(4-(1H-imidazol-1-yl)benzyl)-1H-1,2,4-triazolyl-κ2NN1:N2N)-(μ3-2,2′-(1,2-phenylene)diacetato-κ5-O1,O2:O2:O3,O4)cadmium(II), C22H19CdN5O4
  75. Crystal structure of bis(1-ethyl-6-fluoro-4-oxido-7-(piperazin-1-ium-1-yl)-1,8-naphthyridin-1-ium-3-carboxylate-κ2O,O′)copper(II) benzene-1, 4-dicarboxylate dihydrate, C38H42F2CuN8O12
  76. Redetermination of the crystal structure of potassium lithium molybdate monohydrate, KLiMoO4·H2O
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  78. The crystal structure of tris(μ2-1,3-bis(4,4,4-trifluoro-3-oxido-1-(oxo)but-2-en-1-yl)phenyl-κ4O,O′:O′′,O′′′)-bis(1,2-dimethoxyethane-κ2O,O′)dicerium(III), C50H38F18O16Ce2
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  80. Crystal structure of 2,4-dibenzoyl-N,N-dimethylbenzenamine, C22H19NO2
  81. The crystal structure of 2-(4-methoxyphenyl)-6,8-diphenyl-4-(phenylamino)quinazoline — acetonitrile (1/1), C35H28N4O
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