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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3135Generated: October 23, 2026

4-Methyl-2-nitroaniline → 2-Chloro-6-nitro-p-toluidine

https://huagongshe.com/en/reaction/3135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-2-nitroanilineHCID 6978—
ReactantChlorineHCID 24526—
SolventChloroformHCID 6212—
Product2-Chloro-6-nitro-p-toluidineHCID 7959525%

Reaction Steps

To a stirred solution of 4-methyl-2-nitroaniline (19.69 g, 129.4 mM) in chloroform (200 mL) under a nitrogen atmosphere was added dropwise a solution of chlorine (10.15 g, 285.9 mM) in chloroform (100 mL) while maintaining the reaction mixture temperature below 30° C. The reaction mixture was stirred for 3 days and then washed with aqueous sodium bicarbonate. The organic phase was then concentrated and the residue chromatographed (eluant: hexane/diethyl ether; 9/1) over silica gel to provide (6.03 g, 25%) the title compound as an orange crystalline solid, mp 68.5°-69.5° C.; MS(CI): 187 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733910
Source datasetuspto-grants-1998_03
ORD IDord-29cf4cf9cdd54ff580a9152a0791fb0b
Source noteuspto-grants-1998_03