HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389620Generated: October 25, 2026
Methanol → alpha-Phenylthio-2-thiopheneacetic acid
https://huagongshe.com/reaction/1389620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Product | alpha-Phenylthio-2-thiopheneacetic acid | HCID 23460397 | 41% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04245108 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-dba0232fe8be4cc1b5404907a684d1e4 |
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| Source note | uspto-grants-1981_01 |
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