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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817124Generated: October 29, 2026

Water → 4-(Bromomethyl)-1-methoxy-2-nitrobenzene

https://huagongshe.com/reaction/1817124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl PeroxideHCID 7187—
Reactant1-Methoxy-4-methyl-2-nitrobenzeneHCID 67058—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-1-methoxy-2-nitrobenzeneHCID 1157964870%

Reaction Steps

A solution of 4-methyl-2-nitroanisole (25 mmol), N-bromosuccinimide (25 mmol) and benzoyl peroxide (2.5 mmol) in carbon tetrachloride (100 mL) was heated at reflux for 18 h. The reaction mixture was then poured into water and solid separated was filtered. The aqueous layer was extracted with carbon tetrachloride (3×50 mL) and organic phase was separated and evaporated to give a solid product. The solid products were combined and recrystallized from ethyl acetate-hexane to give a crystalline product of 3-nitro-4-methoxy benzyl bromide. m.p. 110-112° C., yield 70-75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598232B2
Source datasetuspto-grants-2009_10
ORD IDord-f8d79ce5dfe84de481ff891e92a3a05d
Source noteuspto-grants-2009_10