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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441353Generated: October 30, 2026

1-Phenyl-1-propanone → alpha-Ethyl-alpha-phenyl-3-(trifluoromethyl)benzenemethanol

https://huagongshe.com/reaction/441353

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-1-propanoneHCID 7148—
ReactantBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Productalpha-Ethyl-alpha-phenyl-3-(trifluoromethyl)benzenemethanolHCID 41870—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 37.5 g. of propiophenone in 200 ml. of dry ether is added dropwise to a -10° C. Grignard solution prepared from 13.6 g. of magnesium turnings and 126 g. of 3-trifluoromethyl-bromobenzene in 182 ml. of dry ether. The reaction mixture is stirred at 0° C. for 30 minutes, thereafter refluxed for 1 hour. The mixture is cooled to 0° C., and the Grignard complex is decomposed with a 10% aqueous ammonium chloride solution. The etheral phase is separated, washed until neutral, and dried over anhydrous sodium sulfate. The solvent is evaporated, and the residual oil is subjected to fractional distillation in vacuo. This way 57.3 g. of 3-trifluoromethyl-α-ethyl-benzhydrol are obtained; b.p.: 106°-108° C./0.03 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04039589
Source datasetuspto-grants-1977_08
ORD IDord-66c50e8ed13843339ccd23e268e58754
Source noteuspto-grants-1977_08