HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322228Generated: October 26, 2026
Triethylamine → Methyl 3-(3-aminophenylthiomethyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/322228
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminothiophenol | HCID 31577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-(bromomethyl)thiophene-2-carboxylate | HCID 10537693 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-(3-aminophenylthiomethyl)thiophene-2-carboxylate | HCID 15524292 | 92.3% |
Reaction Steps
To a solution of 3-aminothiophenol (2.3 g, 18.7 mmol) and triethylamine (3.12 ml, 22.4 mmol) in dichloromethane (30 ml) was slowly added methyl 3-bromomethylthiophene-2-carboxylate (6.24 g, 22.4 mmol) under ice-cooling, followed by stirring for 30 minutes. After the reaction was completed, a saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture. The organic layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate and a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the organic layer was concentrated under reduced pressure. The obtained oily substance was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give oily methyl 3-(3-aminophenylthiomethyl)thiophene-2-carboxylate (4.82 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211227B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-d51078036d904aeebe883fea751bea90 |
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| Source note | uspto-grants-2001_04 |
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