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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973298Generated: October 26, 2026

4'-Chloro-4-chloromethylbiphenyl → 2-[4-(4-Chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionitrile

https://huagongshe.com/reaction/973298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-Chloro-4-chloromethylbiphenylHCID 12773846—
Reactant2-Hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionitrile sodium saltHCID 86735168—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[4-(4-Chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionitrileHCID 20314462—

Reaction Steps

A solution of 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionitrile sodium salt (4.3 g.) and 4-(4-chlorophenyl)-benzyl chloride (4.7 g.) in dimethylformamide (25 ml.) is stirred at ambient temperature for 10 days, then diluted with water. During this reaction, 2-[4-(4-chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionitrile is formed and is subsequently hydrolysed to the corresponding amide. The mixture is extracted with 1,2,2-trichloro-1,1,2-trifluoroethane, and the extract is dried with sodium sulphate, then evaporated. The residue is crystallised from cyclohexane to give 2-[4-(4-chlorophenyl)benzyloxy]-3,3,3-trifluoro-2-trifluoromethylpropionamide, m.p. 123°-124° C. (1.6 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055595
Source datasetuspto-grants-1977_10
ORD IDord-870e0a4859d441b59a63a61308d443be
Source noteuspto-grants-1977_10