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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198050Generated: October 30, 2026

Methanesulfonyl chloride → N-(3-Bromo-5-(trifluoromethyl)phenyl)methanesulfonamide

https://huagongshe.com/reaction/2198050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
SolventPyridineHCID 1049—
ProductN-(3-Bromo-5-(trifluoromethyl)phenyl)methanesulfonamideHCID 65491442101.1%

Reaction Steps

To a solution of 3-bromo-5-(trifluoromethyl)aniline (10 g) in pyridine (50 ml) was added methanesulfonyl chloride (5.73 g) at 0° C., and the mixture was stirred at room temperature for 16 hr. The reaction mixture was concentrated, saturated aqueous sodium hydrogencarbonate solution was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with 1M hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated to give the title compound (13.4 g, yield quant.) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338622B2
Source datasetuspto-grants-2012_12
ORD IDord-a1dd8330bb0a4079ba08dc4686522053
Source noteuspto-grants-2012_12