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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505671Generated: October 25, 2026

Methanesulfonyl chloride → N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamide

https://huagongshe.com/reaction/505671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
SolventPyridineHCID 1049—
ProductN-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamideHCID 5943090452%

Reaction Steps

To a solution of 2-bromo-5-trifluoromethylaniline (3.18 g, 13.25 mmol) in pyridine (18 ml) was added methanesulfonyl chloride (1.03 ml, 13.25 mmol) and the mixture was stirred for 6 hours at room temperature. The solvent was removed in vacuo and the residue was diluted with chloroform. The organic layer was washed with water, 1N hydrochloric acid, a saturated sodium hydrogen carbonate solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by recrystallization to give the subject compound (2.18 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781479B2
Source datasetuspto-grants-2010_08
ORD IDord-5888ddb31d474185be9e29694440c5d9
Source noteuspto-grants-2010_08