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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515697Generated: October 28, 2026

Thionyl Chloride → 4-(Chloromethyl)-1-(cyclohexylmethyl)-2-(trifluoromethyl)benzene

https://huagongshe.com/reaction/515697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(4-(Cyclohexylmethyl)-3-(trifluoromethyl)phenyl)methanolHCID 67211680—
SolventTolueneHCID 1140—
Product4-(Chloromethyl)-1-(cyclohexylmethyl)-2-(trifluoromethyl)benzeneHCID 67249147100%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of (4-(cyclohexylmethyl)-3-(trifluoromethyl)phenyl)methanol (0.060 g, 0.220 mmol) in toluene (2 mL) was added thionyl chloride (1.32 mmol). The reaction was heated to 75° C. for 3 h and quenched with water at 0° C. The mixture was extracted with hexanes (twice). The combined organics were washed with saturated NaHCO3(aq), dried over MgSO4, and concentrated to give the title compound as an oil (0.220 mmol). 1H NMR (400 MHz, CDCl3) δ ppm 0.91-1.06 (m, 2H), 1.12-1.23 (m, 3H), 1.61-1.74 (m, 6H), 2.66 (d, J=6.95 Hz, 2H), 4.59 (s, 2H), 7.30 (d, J=7.96 Hz, 1H), 7.47 (d, J=7.96 Hz, 1H), 7.63 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108969B2
Source datasetuspto-grants-2015_08
ORD IDord-897cc3b67f094b319fa856663e0df3f8
Source noteuspto-grants-2015_08