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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610262Generated: October 31, 2026

N-bromobutanimide → 1-(Bromomethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzene

https://huagongshe.com/reaction/1610262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantalpha,alpha,beta,beta-Tetrafluoro-p-methylphenetoleHCID 74439—
SolventCarbon TetrachlorideHCID 5943—
Product1-(Bromomethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzeneHCID 22261784—

Reaction Steps

A solution of 4-(1,1,2,2-tetrafluoroethoxy)toluene (6.73 g, 32.3 mmol), N-bromosuccinimide (5.75 g, 32.3 mmol) and 2,2-azobis(isobutyronitrile) (0.2 g) in carbon tetrachloride (30 ml) was heated under reflux for 0.5 hr. After cooling the reaction solution to room temperature, the white precipitate as removed by filtration and the precipitate was washed with diethyl ether. The solvent of the collected filtrate was evaporated under reduced pressure to give a crude product of 4-(1,1,2,2-tetrafluoroethoxy)benzyl bromide as a pale-yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-cb18a0d76d044ff894102acc3746e80d
Source noteuspto-grants-2006_01