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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794132Generated: November 4, 2026

N-bromobutanimide → 1-Bromo-3-(bromomethyl)-2,4-difluorobenzene

https://huagongshe.com/reaction/1794132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Bromo-2,6-difluorotolueneHCID 11287226—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-3-(bromomethyl)-2,4-difluorobenzeneHCID 22220084105.3%

Reaction Steps

Bromo-2,4-difluoro-3-methyl-benzene (22 g, 0.106 M) and N-bromosuccinimide (22.7 g, 0.128 M) were dissolved in tetrachloromethane (800 mL). Dibenzoylperoxide (0.52 g, 2 mM) was added and the mixture was irradiated for 1 h. Succinimide was removed by filtration of the cooled mixture and the filtrate was washed with water. The water phase was extracted with dichloromethane. Organic phases were pooled, dried with MgSO4 and and evaporated to yield a yellowish oil (32 g). The residue was purified by column chromatography (silica gel; n-hexane) to yield 28.4 g (94%) of the title compound as a colorless oil. MS (EI): 286.0 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-843d8c12655c4b1d841861447f58e22a
Source noteuspto-grants-2006_04