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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250284Generated: October 31, 2026

Acetic Anhydride → 4-(Acetylamino)-3-methylbenzoic acid

https://huagongshe.com/reaction/2250284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-Amino-3-methylbenzoic acidHCID 75598—
SolventDichloromethaneHCID 6344—
Product4-(Acetylamino)-3-methylbenzoic acidHCID 301594856%

Reaction Steps

To a suspension of 4-amino-3-methylbenzoic acid (60 g, 0.40 mol) in methylene chloride (800 mL) was added triethylamine (121 g, 1.19 mol). The solution became clear. Then, acetic anhydride (81 g, 0.79 mol) was added and the reaction mixture was stirred for 60 h at room temperature. The solvent was evaporated. The residue was diluted with water (400 mL) and extracted with ethyl acetate (3×600 mL). The combined organic extracts were dried over magnesium sulfate, filtered and evaporated to give the title compound as a tan solid (43 g, 56% yield). 1H-NMR (d6-DMSO, 300 MHz) δ 9.36 (s, 1H), 7.77 (s, 1H), 7.10 (s, 2H), 2.27 (s, 3H), 2.10 (s, 3H). LC/MS: tR=1.22 min, 194 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314883B2
Source datasetuspto-grants-2008_01
ORD IDord-c0ca967093724b2a8d7c7d6e9c94737b
Source noteuspto-grants-2008_01