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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916780Generated: October 30, 2026

2-Methyl-3-nitrobenzoic acid → N-methoxy-N,2-dimethyl-3-nitrobenzamide

https://huagongshe.com/reaction/916780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-nitrobenzoic acidHCID 16096—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
SolventDichloromethaneHCID 6344—
ProductN-methoxy-N,2-dimethyl-3-nitrobenzamideHCID 15338107—

Reaction Steps

Carbonyl diimidazole (9.8 g, 60.7 mmol) was added to a solution of 2-methyl-3-nitrobenzoic acid (10 g, 55 mmol) in CH2Cl2 (200 mL) at 0° C. and stirred for 30 min. The reaction mixture was warmed to room temperature, stirred for 2 h, and cooled to 0 C. N,O-dimethylhydroxylamine hydrochloride was added to the reaction mixture at 0 C, stirred for 30 min., and heated to 45 C for 1 h. The reaction mixture was cooled to room temperature, stirred for 12 h, and quenched with aqueous K2CO3 (10%, 200 mL). The reaction mixture was extracted with CH2Cl2 (3×200 mL) and the combined extracts were dried (MgSO4), filtered, and concentrated in vacuo. Purification by flash column chromatography (silica, 6:4 hexanes:EtOAc) provided the title compound a white solid (2.6 g, 21%). MS: 225 (MH+); HPLC Rf: 3.96 min. (HPLC method 4); HPLC purity: 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271262B2
Source datasetuspto-grants-2007_09
ORD IDord-8a2f085a59964a529adc5d32ba78f5bd
Source noteuspto-grants-2007_09