HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716727Generated: October 25, 2026
Acetic Anhydride → 1-Benzofuran-3-yl acetate
https://huagongshe.com/reaction/716727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Benzoic acid, 2-(carboxymethoxy)- | HCID 69461 | — |
| Product | 1-Benzofuran-3-yl acetate | HCID 2769621 | 76% |
Reaction Steps
To acetic anhydride (300 mL) was added 2-(carboxymethoxy)benzoic acid (7) (100 g, 0.510 mol) at ambient temperature and heated to 130-140° C. The reaction temperature was maintained for 14-20 h under stirring. The progress of the reaction was monitored by the HPLC analysis. Upon completion of the reaction, the reaction mixture was cooled to 50-80° C., acetic anhydride was recovered at 50-80° C. at reduced pressure and the crude product was extracted with dichloromethane (500 mL). The dichloromethane layer was recovered completely to obtain the product meeting the desired specifications. Yield—76-85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193698B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-abcc828987ee480289539a370f4b9825 |
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| Source note | uspto-grants-2015_11 |
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