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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374542Generated: October 26, 2026

Carbon Tetrachloride → 1-(Bromomethyl)-2-chloro-3-methyl-5-nitrobenzene

https://huagongshe.com/reaction/374542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-1,3-dimethyl-5-nitrobenzeneHCID 9920569—
SolventWaterHCID 962—
Product1-(Bromomethyl)-2-chloro-3-methyl-5-nitrobenzeneHCID 1899725070.7%

Reaction Steps

A mixture of 129 g of 2-chloro-1,3-dimethyl-5-nitrobenzene, 125 g of 1-bromo-2,5-pyrrolidinedione, 12 g of dibenzoyl peroxide and 1200 ml of tetrachloromethane was stirred for 2 hours at reflux temperature using a water separator. Twice there was added an extra portion of 20 g of dibenzoyl peroxide during a refluxing period of 29 hours. After cooling, the reaction mixture was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /hexane 50:50). The eluent of the desired fraction was evaporated, yielding 130 g (70.2%) of 1-(bromomethyl)-2-chloro-3-methyl-5-nitrobenzene (interm. 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05480912
Source datasetuspto-grants-1996_01
ORD IDord-a2d6793df1834518a51fc3a7edf07cbf
Source noteuspto-grants-1996_01