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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491412Generated: October 25, 2026

N-bromobutanimide → 2-Bromo-4-(bromomethyl)-1-methoxybenzene

https://huagongshe.com/reaction/491412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-4-methylanisoleHCID 89143—
CatalystAzobisisobutyronitrileHCID 6547—
Product2-Bromo-4-(bromomethyl)-1-methoxybenzeneHCID 11277462100%

Reaction Steps

2-Bromo-4-methyl anisole 14 (2.2 mL, 14.9 mmol) was dissolved in dichlomethane (30 mL) and N-bromosuccinimide (3.75 g, 16.4 mmol) was added followed by AIBN (26.0 mg). The reaction was heated to reflux for 19 hrs., then cooled to room temperature and the precipitate was filtered off. The filtrate was diluted with dichloromethane and washed with 0.5 M aqueous sodium bicarbonate, followed by water. The organic mixture was dried over sodium sulfate, filtered and concentrated under vacuum to yield 15 (4.16 g, 100%). The benzyl bromide was used as the crude material without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531544B2
Source datasetuspto-grants-2009_05
ORD IDord-5109376a568e483292ffa4820f2aa5f8
Source noteuspto-grants-2009_05