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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572128Generated: October 26, 2026

O-Toluidine → N-acetyl-o-toluidine

https://huagongshe.com/reaction/572128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantAcetic AnhydrideHCID 7918—
SolventDichloromethaneHCID 6344—
ProductN-acetyl-o-toluidineHCID 844395.4%

Reaction Steps

Acetic anhydride (33.0 mL, 350 mmol) was added to a stirred solution of o-toluidine (30.0 g, 280 mmol) in dichloromethane (500 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 20 h. The reaction mixture was partitioned between DCM and water. The organic phase was washed with brine, then dried (MgSO4) and evaporated in vacuo. The residue was stirred in isohexane at 0° C. for 2 h, then filtered. The precipitate was washed with isohexane and dried under vacuum. The title compound (39.87 g, 95%) was obtained as a pale pink solid. δH (CDCl3) 7.80-7.78 (m, 1H), 7.26-7.20 (m, 2H), 7.13-7.08 (m, 1H), 6.92 (br s, 1H), 2.29 (s, 3H), 2.23 (s, 3H). LCMS (ES+) 150 (M+H)+, RT 0.85 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029392B2
Source datasetuspto-grants-2015_05
ORD IDord-43e33d2d18e34937aed4d07318fdf924
Source noteuspto-grants-2015_05