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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216698Generated: October 30, 2026

Acetic Anhydride → Acetic acid 5-bromo-2-methyl-benzofuran-3-yl ester

https://huagongshe.com/reaction/216698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium AcetateHCID 517045—
Reactant5-Bromo-2-(1-carboxy-ethoxy)-benzoic acidHCID 59192027—
ProductAcetic acid 5-bromo-2-methyl-benzofuran-3-yl esterHCID 5919203665%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 5-bromo-2-(1-carboxy-ethoxy)-benzoic acid (31.2 g, 108 mmol), acetic anhydride (216 mL) and anhydrous sodium acetate (21.8 g, 266 mmol) is heated under reflux (150° C.) for 4 h. After cooling to room temperature the reaction mixture is carefully quenched with ice-cold water (500 mL). A white precipitate is formed which is collected by suction filtration, thoroughly washed with water and dried in vacuo at 45° C. to afford the title compound as a white powder (19.0 g, 70.6 mmol, 65%). MS (ES+): 269 (M(C11H979BrO3)+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193236B2
Source datasetuspto-grants-2012_06
ORD IDord-cb4ca9c40d384ad292cf3b0ac49a6aa3
Source noteuspto-grants-2012_06