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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717000Generated: November 1, 2026

N-bromobutanimide → 2-Bromo-5-methoxybenzyl bromide

https://huagongshe.com/reaction/717000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-Bromo-4-methoxy-2-methylbenzeneHCID 117915—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-5-methoxybenzyl bromideHCID 3525951—

Reaction Steps

Into a 1000-mL round-bottom flask, was placed a solution of 1-bromo-4-methoxy-2-methylbenzene (20 g, 100.00 mmol, 1.00 equiv) in CCl4 (200 mL). Then NBS (19.58 g, 110.00 mmol, 1.10 equiv) and BPO (1.21 g, 5.00 mmol, 0.05 equiv) were added. The resulting solution was heated to reflux for 7 hs in an oil bath. The resulting solids were filtered out. The filtrate was concentrated under vacuum and applied onto a silica gel column with ethyl acetate/petroleum ether (1:500). This resulted in 5.9 g (21%) of 1-bromo-2-(bromomethyl)-4-methoxybenzene as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193693B2
Source datasetuspto-grants-2015_11
ORD IDord-b9fbbbffdddb4ba28dce0fab9534ed1d
Source noteuspto-grants-2015_11