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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437829Generated: October 30, 2026

Hydrochloric Acid → 4-Chloro-2-(3-trifluoromethyl-phenoxy)-benzyl alcohol

https://huagongshe.com/reaction/437829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium borohydrideHCID 4148881—
Reactant4-Chloro-2-(3-trifluoromethylphenoxy)-benzoic acid methyl esterHCID 54008629—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-2-(3-trifluoromethyl-phenoxy)-benzyl alcoholHCID 54408113—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 103 g. of 4-chloro-2-(3-trifluoromethyl-phenoxy)-benzoic acid methyl ester in 400 ml. of tetrahydrofuran is added dropwise at reflux over a period of 30 minutes to a solution of 16.2 g. of lithium borohydride in 280 ml. of absolute tetrahydrofuran. The mixture is then cooled to 0° C. and slowly added dropwise to 400 ml. of 3-N aqueous hydrochloric acid. After the addition of 500 ml. of water, the mixture is extracted twice with ether. After evaporation of the ether, there is obtained 4-chloro-2-(3-trifluoromethyl-phenoxy)-benzyl alcohol in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04032525
Source datasetuspto-grants-1977_06
ORD IDord-66b91c9763434a928187bf5fcf85df48
Source noteuspto-grants-1977_06