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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501035Generated: November 2, 2026

Trifluoroacetic acid → 3-Methyl-4-phenoxybenzoic acid

https://huagongshe.com/reaction/1501035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 3-methyl-4-phenoxybenzoateHCID 89581022—
SolventDichloromethaneHCID 6344—
Product3-Methyl-4-phenoxybenzoic acidHCID 2064605838.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of tert-butyl 3-methyl-4-phenoxybenzoate (654 mg, 2.3 mmol), 2,2,2-trifluoroacetic acid (1 mL) and dichloromethane (4 mL) were stirred at 20° C. for 4 hours. The mixture was washed with water (10 mL×2). The organic phase was separated, dried over sodium sulfate, filtered and concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=2:1) to give 3-methyl-4-phenoxybenzoic acid as a white solid (200 mg, 38%). LRMS (M+H)− m/z: calcd 228.08. found 228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-e654d2879caa499590f796fbabc79d49
Source noteuspto-grants-2015_12