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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380015Generated: November 1, 2026

N-bromobutanimide → 4-(Bromomethyl)-3-trifluoromethylbenzenesulphonyl chloride

https://huagongshe.com/reaction/2380015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methyl-3-(trifluoromethyl)benzene-1-sulfonyl chlorideHCID 18956556—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-3-trifluoromethylbenzenesulphonyl chlorideHCID 18956552—

Reaction Steps

64.6 g (0.25 mol) of 3-trifluoromethyl-4-methylbenzenesulphonyl chloride are taken up in 500 ml of carbon tetrachloride and, after addition of 44.5 g (0.25 mol) of N-bromosuccinimide and 0.4 g of ABN, the mixture is heated under reflux for 24 hours. After cooling, the solids are filtered off and the filtrate is freed from the solvent. Flash chromatography using petroleum ether/toluene (4:1), 50 μm particle size, gives 33.9 g (40% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364942
Source datasetuspto-grants-1994_11
ORD IDord-4bd4ee4c3f2f43db8ef12b2d3b3005f6
Source noteuspto-grants-1994_11