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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 5-Bromo-2-(1-carboxy-ethoxy)-benzoic acid | HCID 59192027 | — |
| Product | Acetic acid 5-bromo-2-methyl-benzofuran-3-yl ester | HCID 59192036 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193236B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-cb4ca9c40d384ad292cf3b0ac49a6aa3 |
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| Source note | uspto-grants-2012_06 |
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