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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427100Generated: November 3, 2026

Acetic Anhydride → 2-Acetamido-3-methylbenzoic acid

https://huagongshe.com/reaction/2427100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Amino-3-methylbenzoic acidHCID 78101—
SolventWaterHCID 962—
Product2-Acetamido-3-methylbenzoic acidHCID 1263920438%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.51 g of 2-amino-3-methylbenzoic acid, 1.0 g of acetic anhydride and 20 ml of tetrahydrofuran was stirred at 80° C. for 13 hours. The reaction mixture was allowed to cool to room temperature, poured into water, and extracted with ethyl acetate two times. The organic layers were combined, washed successively with water and an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was washed with ethyl acetate to obtain 0.72 g of 2-acetylamino-3-methylbenzoic acid of the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968573B2
Source datasetuspto-grants-2011_06
ORD IDord-dc0d8bc0053f4d54b7eb9f859b96b776
Source noteuspto-grants-2011_06