HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6125Generated: October 26, 2026
Oxalyl chloride → 3-Methyl-2-thenoyl Chloride
https://huagongshe.com/reaction/6125
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Methyl-2-thenoic acid | HCID 90269 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Methyl-2-thenoyl Chloride | HCID 2737605 | 100.3% |
Reaction Steps
In 100 ml of benzene was suspended 3.00 g (21.1 mmol) of 3-methyl-2-thiophenecarboxylic acid, oxalyl chloride [7.36 ml (84.4 mmol)] was added and the mixture was refluxed for 2 hours. After cooling, the solvent was distilled off to obtain 3.40 g of 3-methylthenoyl chloride (yield: quant.). To a solution of 1.50 g (6.23 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride and 2.61 ml (18.7 mmol) of triethylamine in 60 ml of methylene chloride, 1.20 ml (7.48 mmol) of the 3-methylthenoyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain powder. The powder was washed with ether and dried to obtain 1.54 g of the desired compound (yield: 84.5%, pale yellow powder).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246948 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-e04cbcb18b1d47e8b7a7115f33cccf17 |
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| Source note | uspto-grants-1993_09 |
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