Home Crystal structure of (Z)-2-bromo-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-phenylprop-2-en-1-one, C23H27BrO2
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Crystal structure of (Z)-2-bromo-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-phenylprop-2-en-1-one, C23H27BrO2

  • Ali N. Khalilov , Ayten R. Asgarova , Atash V. Gurbanov , Abel M. Maharramov , Farid N. Nagiyev and Iván Brito EMAIL logo
Published/Copyright: September 5, 2018

Abstract

C23H27BrO2, P21/n (no. 14), a = 10.3200(18) Å, b = 15.905(3)(6) Å, c = 12.913(2) Å, β = 97.683(4), V = 2100.6(6) Å3, Z = 4, Rgt(F) = 0.0319, wRref(F2) = 0.0872, T = 296(2) K.

CCDC no.: 1862075

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 prism
Size:0.17 × 0.15 × 0.15 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:1.97 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω
θmax, completeness:27.0°, >99%
N(hkl)measured, N(hkl)unique, Rint:21854, 4591, 0.022
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3732
N(param)refined:241
Programs:Bruker [1], SHELX [2], Olex2 [3]
Table 2:

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

AtomxyzUiso*/Ueq
Br10.72766(2)0.11800(2)0.95063(2)0.04809(9)
O10.68221(17)0.02921(12)0.74815(15)0.0646(5)
O20.2748(2)0.31050(11)1.21175(16)0.0750(6)
H2O0.31360.35841.21330.113*
C10.4684(2)−0.02245(13)0.73662(15)0.0396(4)
C20.3873(2)−0.06645(14)0.79337(17)0.0468(5)
H2A0.3974−0.06140.86580.056*
C30.2910(3)−0.11803(16)0.7434(2)0.0629(7)
H3A0.2366−0.14740.78240.075*
C40.2749(3)−0.12634(19)0.6372(3)0.0729(8)
H4A0.2095−0.16090.60390.087*
C50.3556(4)−0.0836(2)0.5804(2)0.0854(10)
H5A0.3455−0.08930.50810.102*
C60.4512(3)−0.0323(2)0.6291(2)0.0727(8)
H6A0.5057−0.00360.58940.087*
C70.5797(2)0.03023(13)0.78504(16)0.0415(5)
C80.56493(19)0.08382(13)0.87725(15)0.0364(4)
C90.4505(2)0.10827(13)0.90392(16)0.0388(4)
H9A0.37900.08570.86150.047*
C100.41368(19)0.16345(13)0.98636(15)0.0375(4)
C110.4870(2)0.23193(13)1.02806(16)0.0401(4)
H11A0.56580.24391.00360.048*
C120.4467(2)0.28288(13)1.10493(16)0.0394(4)
C130.3266(2)0.26307(13)1.13903(16)0.0422(5)
C140.2498(2)0.19411(13)1.10084(16)0.0408(5)
C150.2956(2)0.14626(14)1.02373(17)0.0400(4)
H15A0.24580.10090.99580.048*
C160.5316(2)0.35910(15)1.14972(19)0.0489(5)
C170.6586(3)0.3630(2)1.1025(3)0.0834(10)
H17A0.70920.41031.13100.125*
H17B0.63950.36911.02810.125*
H17C0.70740.31221.11870.125*
C180.5654(4)0.3497(2)1.2696(3)0.0868(10)
H18A0.59460.40281.29940.130*
H18B0.63350.30871.28500.130*
H18C0.48910.33191.29870.130*
C190.4611(3)0.44145(15)1.1238(2)0.0626(7)
H19A0.52250.48301.10710.094*
H19B0.42120.45991.18280.094*
H19C0.39490.43361.06490.094*
C200.1187(2)0.17365(15)1.1410(2)0.0514(6)
C210.1387(3)0.16141(19)1.2597(2)0.0716(8)
H21A0.20540.12001.27830.107*
H21B0.05830.14281.28200.107*
H21C0.16480.21371.29320.107*
C220.0199(3)0.24498(19)1.1092(3)0.0796(9)
H22A0.00800.25111.03450.119*
H22B0.05260.29671.14100.119*
H22C−0.06240.23151.13220.119*
C230.0592(2)0.09225(17)1.0920(2)0.0616(7)
H23A0.11910.04661.10910.092*
H23B0.04240.09861.01750.092*
H23C−0.02140.08061.11880.092*

Source of material

The title compound was prepared by dropwise addition of bromine (1.25 mmol) to 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-phenyl-propenone (1.19 mmol) in methylene chloride (10 mL) and the reaction mixture was stirred for three hours at room temperature. The reaction mixture was evaporated. The raw product was recrystallized in ethanol to get crystals. The yield of the title compound is 70% m.p. 148 °C; 1H NMR (300 MHz, DMSO-d6) δ 1.41 (s, 18H, 6CH3), 7.48–7.84 (m, 9H, 5CHarom + 2CHarom + CH = +OHarom). 13C NMR (75 MHz, CDCl3) δ 30.92 (6CH3), 35.05 (2Cquat.), 119.07 (Carom ), 124.80 (Carom), 128.52 (CHarom), 129.36 (CHarom), 129.82 (CHarom), 132.86 (CHarom), 137.32 (Carom), 138.90 (Carom), 145.19 (CH=), 157.21 (=Cquat.), 191.38 (C = O).

Experimental details

H atoms were located in the difference Fourier map, but refined with fixed individual displacement parameters, using a riding model with C—H distances of 0.93 Å (for aromatic rings), 0.96 Å (CH3 group), with U(H) values of 1.2Ueq(C) (for CH in aromatic moiety), and 1.5Ueq(C) (for CH3) and O—H distance 0.8601 Å, with U(H) values of 1.2Ueq(O).

Comment

α-Halogen chalcones are valuable synthetic building blocks in organic synthesis [4, 5] . The existence of bulky and electron-withdrawing groups in α-position lead to an enhancement of the electrophilicity. Examples of the influence of α-modification on biological activity was presented in literature. α-Halo chalcones are shown to possess biological activity [6]. Development of chalcones and related analogues as antimitotic agents was reported [7].

In the title compound the dihedral angle between the mean planes of the aromatic rings is 40.36(12)°. A search in the latest version of the Cambridge structural database, for related compounds yielded only one structure namely 3-(3,5-di-t-butyl-4-hydroxyphenyl)-1-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one (REFCODE PASSOU) [8]. The geometrical and molecular parameters are very similar between both compounds and the main difference is the crystal packing. In the title compound the molecules are linked by van der Waals interactions only, whereas in the related compound, the molecules are linked by hydrogen bond interactions. The conformation about the C=C bond is Z, with a C7—C8—C9—C10 torsion angle of 176.26(3)°.

Acknowledgements

Ali Khalilov thankful to Baku State University for the “50+50” individual grant support in this work.

References

Bruker. APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, WI, USA (2005).Search in Google Scholar

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Dolomanov, O. V.; Bourhis, L. J.; Gildea, R. J.; Howard, J. A. K.; Puschmann, H.: OLEX2: a complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 42 (2009) 339–341.10.1107/S0021889808042726Search in Google Scholar

Ramanarayanan, G. V.; Shukla, V. G.; Akamanchi, K. G.: A novel and one step procedure for preparation of α-bromo-α, β-unsaturated carbonyl compounds. Synlett 12 (2002) 2059–2061.10.1002/chin.200310051Search in Google Scholar

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Received: 2018-04-09
Accepted: 2018-08-14
Published Online: 2018-09-05
Published in Print: 2018-11-27

©2018 Ali N. Khalilov et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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