HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643776Generated: October 31, 2026
Sodium Acetate → Ethyl 7-(Acetyloxy)-2-methyl-1-benzothiophene-5-carboxylate
https://huagongshe.com/reaction/1643776
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-(Ethoxycarbonyl)-4-(5-methyl-3-thienyl)but-3-enoic Acid | HCID 66755556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | Ethyl 7-(Acetyloxy)-2-methyl-1-benzothiophene-5-carboxylate | HCID 59560166 | 42% |
Reaction Steps
Sodium acetate (30 g, 0.36 mol) was added under vigorous stirring to a solution of 3-(ethoxycarbonyl)-4-(5-methyl-3-thienyl)but-3-enoic acid (30 g, 0.12 mol) in 300 mL of acetic anhydride. The reaction mixture was refluxed for 3 h and evaporated in vacuum (˜20 mmHg) at 70° C. until the solvent distillation ceased. The obtained crude product was suspended in 500 mL of dichloromethane. The suspension was filtered. The precipitate was washed by 250 mL of dichloromethane. The combined solutions were washed by 350 mL of a saturated aqueous solution of NaHCO3 and evaporated in vacuum to dryness. The obtained crude product was chromatographed on a layer of silica gel (250×150 mm) with hexane/ethyl acetate mixture (3:1) to give the desired product 14 g (50 mmol, 42%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119624B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-31a83d9989f5474481522699a3ab1489 |
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| Source note | uspto-grants-2012_02 |
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