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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086565Generated: October 27, 2026

N-bromobutanimide → 4-(Bromomethyl)-3-methoxybenzonitrile

https://huagongshe.com/reaction/1086565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Methoxy-4-methylbenzonitrileHCID 14752994—
CatalystBenzoyl PeroxideHCID 7187—
CatalystTungstenHCID 23964—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-3-methoxybenzonitrileHCID 1475299565%

Reaction Steps

N-Bromosuccinimide (3.2 g.) and benzoyl peroxide (0.005 g.) were added to a solution of 3-methoxy-4-methylbenzonitrile (2.65 g.) in dry carbon tetrachloride (90 ml.). The mixture was heated to reflux for 15 minutes using a 250 watt tungsten lamp. The cooled reaction mixture was diluted with petrolum ether (b.p. 60°-80° C., 90 ml.), insoluble material removed by filtration, and the filtrate evaporated. The solid residue was recrystallized from a mixture of dichloromethane and petroleum ether to give 4-bromomethyl-3-methoxybenzonitrile (W) (2.64 g., 65%) as a white solid, m.p. 87°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030643
Source datasetuspto-grants-1991_07
ORD IDord-bf0a5a5d1fc647c5824c427e22b8c39f
Source noteuspto-grants-1991_07