HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27593Generated: October 26, 2026
Methanol → alpha-Phenylthio-2-thiopheneacetic acid
https://huagongshe.com/reaction/27593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | alpha-Trichloromethyl-2-thiophenemethanol | HCID 12566320 | — |
| Product | alpha-Phenylthio-2-thiopheneacetic acid | HCID 23460397 | 76% |
Reaction Steps
Under an argon atmosphere, potassium hydroxide (1.12 g, 20 mmol) was dissolved in methanol (10 ml). Thiophenol (0.6 g, 5.45 mmol) was added to this solution with stirring and under water cooling. After 10 min., a solution of α-trichloromethyl-2-thiophenemethanol (1.16 g, 5 mmol) in methanol (3 ml) was added. After 10 min., the mixture was gradually heated up and was heated under reflux for 2 hr. with vigorous stirring. After cooling to room temperature and after removal of most of the solvent by distillation under a reduced pressure, diethylether was added and the mixture was decomposed with dilute hydrochloric acid. The ether layer was separated, washed with water, and dried with anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under a reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate: n-hexane=1:4) to give 940 mg of α-phenylthio-2-thiopheneacetic acid as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04221915 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-c49a5a66e8e9498c8e752722cf12a997 |
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| Source note | uspto-grants-1980_09 |
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