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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643727Generated: November 2, 2026

Sodium Acetate → 6-Benzofurancarboxylic acid, 4-(acetyloxy)-2-methyl-, ethyl ester

https://huagongshe.com/reaction/1643727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant3-(Ethoxycarbonyl)-4-(5-methyl-2-furyl)but-3-enoic AcidHCID 66755912—
SolventDichloromethaneHCID 6344—
SolventAcetic AnhydrideHCID 7918—
Product6-Benzofurancarboxylic acid, 4-(acetyloxy)-2-methyl-, ethyl esterHCID 5956009451%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-9587f1e1c4be47cb8d9479c47b183448
Source noteuspto-grants-2012_02