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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015362Generated: October 25, 2026

Trifluoroacetic acid → 4-(2-Fluorobenzyl)cyclohexanecarboxylic Acid Methyl Ester

https://huagongshe.com/reaction/1015362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactant4-(2-Fluorobenzoyl)cyclohexanecarboxylic Acid Methyl EsterHCID 57516873—
Product4-(2-Fluorobenzyl)cyclohexanecarboxylic Acid Methyl EsterHCID 6730203683.2%

Reaction Steps

In an 18 mL vial with stir bar and 4-(2-fluorobenzoyl)cyclohexanecarboxylic acid methyl ester (333 mg; 1.2 mmol), trifluoroacetic acid (4 mL) was chilled to 0° C. and triethylsilane (700 mg; 6.0 mmol) was added over 1 minute. Mixture was allowed to warm to room temperature. After 48 hours, mixture was concentrated in vacuo and reduced by half volume. Mixture was poured into cold KOH solution and pH adjust further to pH 6. Aqueous mixture was extracted 3×5 mL ethyl acetate. Combined ethyl acetate was washed with brine and dried over MgSO4. Crude oil was purified via (20:1) flash chromatography 0-10% ethyl acetate in hexanes to give 250 mg of title compound. (83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985755B2
Source datasetuspto-grants-2011_07
ORD IDord-eb8677f7660f4a8b9165adf123a9adfd
Source noteuspto-grants-2011_07