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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040557Generated: October 31, 2026

Water → 4-(Bromomethyl)-1-(cyclohexylmethyl)-2-(trifluoromethyl)benzene

https://huagongshe.com/reaction/2040557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus tribromideHCID 24614—
Reactant(4-(Cyclohexylmethyl)-3-(trifluoromethyl)phenyl)methanolHCID 67211680—
SolventDichloromethaneHCID 6344—
Product4-(Bromomethyl)-1-(cyclohexylmethyl)-2-(trifluoromethyl)benzeneHCID 67210891198.9%

Reaction Steps

To a stirred solution of (4-(cyclohexylmethyl)-3-(trifluoromethyl)phenyl)methanol (80 mg, 0.29 mmol) in dry DCM (1 mL) was added tribromophosphine (11 μL, 0.12 mmol) at 0° C. The reaction mixture was slowly warmed to room temperature and stirred for 1 h, poured into water, extracted with DCM. The combined organics were washed with saturated NaHCO3 solution and brine, dried and concentrated. The residue was purified by column chromatography to give the title compound (80 mg) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 0.96-1.06 (m, 2H), 1.14-1.22 (m, 3H), 1.55-1.72 (m, 6H), 2.65 (d, J=6.5 Hz, 2H), 4.49 (s, 2H), 7.28 (d, J=8.0 Hz, 1H), 7.47 (dd, J=8.0 and 1.7 Hz, 1H), 7.63 (d, J=1.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580841B2
Source datasetuspto-grants-2013_11
ORD IDord-778700b12ccc4b0e8d4d1d6408f016a5
Source noteuspto-grants-2013_11