HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177253Generated: October 31, 2026
Sodium Acetate → 6-Benzofurancarboxylic acid, 4-(acetyloxy)-2-methyl-, ethyl ester
https://huagongshe.com/reaction/1177253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-(Ethoxycarbonyl)-4-(5-methyl-2-furyl)but-3-enoic Acid | HCID 66755912 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 6-Benzofurancarboxylic acid, 4-(acetyloxy)-2-methyl-, ethyl ester | HCID 59560094 | 51% |
Reaction Steps
Sodium acetate (30 g, 0.36 mol) was added under vigorous stirring to a solution of 3-(ethoxycarbonyl)-4-(5-methyl-2-furyl)but-3-enoic acid (45 g, 0.19 mol) in 250 mL of acetic anhydride. The reaction mixture was refluxed for 2 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 solid was washed with 200 mL of dichloromethane. The combined solutions were washed with 200 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 (200×150 mm) with hexane/ethyl acetate mixture, 3:1 as eluent to give 25 g (95 mmol, 51%) of desired compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842713B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-23ab55de58a94ed9acd3abde4ab101fe |
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| Source note | uspto-grants-2010_11 |
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