Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658508Generated: November 2, 2026

Benzoyl Peroxide → 3',4'-Dichloro-2-fluoro-4-bromomethyl-biphenyl

https://huagongshe.com/reaction/658508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantSodium SulfiteHCID 24437—
ReactantN-bromobutanimideHCID 67184—
Reactant3',4'-Dichloro-2-fluoro-4-methyl-biphenylHCID 66916736—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3',4'-Dichloro-2-fluoro-4-bromomethyl-biphenylHCID 66916717—

Reaction Steps

3′,4′-dichloro-2-fluoro-4-methyl-biphenyl (29 g, 0.114 mol), N-bromosuccinimide (21.2 g, 0.119 mol), benzoyl peroxide (1.4 g, 0.004 mol) were dissolved in acetonitrile (190 ml). The mixture was refluxed for 3 hours, then cooled, mixed with a solution of sodium sulphite (2.2 g) in water (54 ml), stirred for 30 minutes and then allowed to rest to separate the phases. The lower aqueous phase was separated and extracted with dichloromethane (29 ml). The upper phase was concentrated under vacuum, mixed with water (10 ml), and dichloromethane (58 ml) and stirred. The organic phases were separated and put together, washed twice with water (29 ml), and concentrated under vacuum. The compound 3′,4′-dichloro-2-fluoro-4-bromomethyl-biphenyl was isolated as an orange oil (35.7 g, 94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076505B2
Source datasetuspto-grants-2011_12
ORD IDord-04476d7e230b45209aca6cae7e8145c6
Source noteuspto-grants-2011_12