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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995143Generated: October 30, 2026

N-bromobutanimide → 2-Bromo-1-bromomethyl-3-nitrobenzene

https://huagongshe.com/reaction/1995143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-3-nitrotolueneHCID 231828—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-1-bromomethyl-3-nitrobenzeneHCID 1106634290.4%

Reaction Steps

A stirred solution of 1-bromo-2-methyl-6-nitrobenzene (16.2 g, 0.075 mole) in 200 ml of carbon tetrachloride was irradiated and heated at reflux with a 250 watt brooder lamp. N-bromosuccinimide (13.5 g, 0.075 mole) was added to the refluxing reaction mixture, and the mixture was stirred for approximately 23 hours. The mixture was cooled, filtered, and washed with two 200 ml portions of saturated aqueous sodium chloride solution. The organic phase was passed through phase separation filter paper. The filtrate was evaporated under reduced pressure to give 2-bromo-1-bromomethyl-3-nitrobenzene (20 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402973
Source datasetuspto-grants-1983_09
ORD IDord-663fdc46f08e42b3a6b0e9eba83ffc47
Source noteuspto-grants-1983_09