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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532661Generated: November 1, 2026

4-Chloro-3-nitrobenzoic acid → 4-chloro-N-methyl-3-nitrobenzamide

https://huagongshe.com/reaction/1532661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-nitrobenzoic acidHCID 7320—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventDimethylformamideHCID 6228—
Product4-chloro-N-methyl-3-nitrobenzamideHCID 799286—

Reaction Steps

Thionyl chloride (0.65 ml) was added to a solution containing 4-chloro-3-nitrobenzoic acid (1.50 g) in N,N-dimethylformamide (15 ml) and stirred for 30 minutes at room temperature. Methylamine hydrochloride (1.21 g) and triethylamine (3.11 ml) were added to the reaction mixture. After being stirred for 1 hour at room temperature, the reaction mixture was concentrated. The residue, with ethyl acetate added thereto, was washed with water, 1N sodium hydroxide aqueous solution, 1N hydrochloric acid aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated. The yellow solid residue was purified by silica gel column chromatography (silica gel 10 g, chloroform:methanol=1:0-10:1), thereby yielding the entitled compound (0.97 g) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204264B1
Source datasetuspto-grants-2001_03
ORD IDord-280327f4c0044d9bbcecb213aea13b42
Source noteuspto-grants-2001_03