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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964115Generated: October 29, 2026

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

https://huagongshe.com/reaction/1964115

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 numberUS08415484B2
Source datasetuspto-grants-2013_04
ORD IDord-8cc1b6617ef84787a925d4a1b3ec4295
Source noteuspto-grants-2013_04