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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552269Generated: October 30, 2026

4-Phenyl-5-(trifluoromethyl)thiophene-2-carboxylic acid → 1-[4-phenyl-5-(trifluoromethyl)-2-thienyl]ethan-1-one

https://huagongshe.com/reaction/552269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenyl-5-(trifluoromethyl)thiophene-2-carboxylic acidHCID 2783372—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product1-[4-phenyl-5-(trifluoromethyl)-2-thienyl]ethan-1-oneHCID 2740139—

Reaction Steps

To a solution of 4-phenyl-5-trifluoromethyl-thiophene-2-carboxylic acid (272 mg, 1.0 mmol) in THF (10 mL), a solution of MeLi (1.30 mL, 1.6 M solution in diethyl ether) is added. The dark red reaction mixture is stirred at it for 10 min. The reaction is quenched by adding sat. aq. NH4Cl (10 mL). The organic phase is separated, dried over Na2SO4 and evaporated. The crude product is purified by prep. HPLC (Waters Xterra MS18, 75×30 mm, 10 μm, 10 to 95% acetonitrile in water containing 0.5% formic acid) to give 1-(4-phenyl-5-trifluoromethyl-thiophen-2-yl)-ethanone (31 mg) as pale yellow oil, LC-MS: tR=1.06 min, 1H NMR (CDCl3): δ 7.62-7.60 (m, 1H), 7.45-7.40 (m, 5H), 2.60 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951794B2
Source datasetuspto-grants-2011_05
ORD IDord-41fde636b53a4103a83c45270e2c376c
Source noteuspto-grants-2011_05