Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353633Generated: October 31, 2026

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

https://huagongshe.com/reaction/1353633

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 3H). LC/MS: tR=1.22 min, 194 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220862B2
Source datasetuspto-grants-2007_05
ORD IDord-3a6b952782fd4b8ea031a762d6d48de8
Source noteuspto-grants-2007_05