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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantBenzoic acid, 2-(carboxymethoxy)-HCID 69461—
Product1-Benzofuran-3-yl acetateHCID 276962176%

Reaction Conditions

Temperature135 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193698B2
Source datasetuspto-grants-2015_11
ORD IDord-abcc828987ee480289539a370f4b9825
Source noteuspto-grants-2015_11