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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389620Generated: October 25, 2026

Methanol → alpha-Phenylthio-2-thiopheneacetic acid

https://huagongshe.com/reaction/1389620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChloroformHCID 6212—
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantThiophenolHCID 7969—
ReactantPotassium HydroxideHCID 14797—
Productalpha-Phenylthio-2-thiopheneacetic acidHCID 2346039741%

Reaction Steps

6.80 g (103 mmols) of potassium hydroxide (85% purity) was dissolved in 20 ml of methanol, and the resulting solution was added dropwise to a solution of 2.24 g (20.0 mmols) of thiophenealdehyde, 3.5 g (30.0 mmols) of chloroform and 3.30 g (30 mmols) of thiophenol in 10 ml of methanol over a period of 30 minutes at room temperature. The resulting reaction mixture was stirred at room temperature for 1 hour, and heated while refluxing for 1 hour. Most of the solvent was removed by distillation under reduced pressure, and the residue was dissolved in water. The solution was rendered acidic with hydrochloric acid, and extracted with methylene chloride. The organic layer was dried over anhydrous magnesium sulfate and purified by silica gel column chromatography eluting with diethyl ether-hexane (1:5 by volume) to obtain 2.03 g (41% yield) of α-phenylthiothiophene-2-acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04245108
Source datasetuspto-grants-1981_01
ORD IDord-dba0232fe8be4cc1b5404907a684d1e4
Source noteuspto-grants-1981_01