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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552267Generated: October 25, 2026

Ethyl Thioglycolate → Ethyl 4-phenyl-5-(trifluoromethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/552267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
Reactant3-Chloro-4,4,4-trifluoro-2-phenyl-but-2-enalHCID 53396122—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductEthyl 4-phenyl-5-(trifluoromethyl)thiophene-2-carboxylateHCID 278147556.2%

Reaction Steps

To a solution of ethyl 2-mercaptoacetate (0.88 g, 6.75 mmol) in THF (45 mL) NaH (271 mg, 6.75 mmol, 60% in mineral oil) is added at −10° C. The mixture is stirred at 0° C. for 30 min before a solution of 3-chloro-4,4,4-trifluoro-2-phenyl-but-2-enal 1.32 g (4.5 mmol) in THF (5 mL) is added. The reaction mixture is stirred at it for 45 min, then treated with 2 N aq. NaOH (2 mL). Stirring is continued for 15 min and the mixture is diluted with water (100 mL) and 1 N aq. NaOH (15 mL). The mixture is extracted with diethyl ether (70 mL). The organic extract is 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 4-phenyl-5-trifluoromethyl-thiophene-2-carboxylic acid ethyl ester (760 mg) as a brownish oil, LC-MS: tR=1.12 min; 1H NMR (CDCl3): δ 7.75-7.72 (m, 1H), 7.42 (s, 5H), 4.39 (q, J=7.0 Hz, 2H), 1.40 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951794B2
Source datasetuspto-grants-2011_05
ORD IDord-bd0bbe12910c41dcb25c780f3c68101c
Source noteuspto-grants-2011_05