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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070955Generated: October 31, 2026

Methanesulfonyl chloride → N-(3-bromo-5-cyanophenyl)methanesulfonamide

https://huagongshe.com/reaction/2070955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Amino-5-bromobenzonitrileHCID 53406961—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(3-bromo-5-cyanophenyl)methanesulfonamideHCID 6867010188%

Reaction Steps

To a stirring solution of 502 mg of 3-amino-5-bromobenzonitrile in 6 mL of CH2Cl2 and 2 mL of pyridine at 0° C. was added 0.2 mL (2.57 mmol) of MsCl at 0° C. The ice bath was removed and stirring was continued at r.t. for 6.5 h. The solution was concentrated and EtOAc and 20 mL of H2O were added. The organic layer was washed with 15 mL of brine and water, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (35% EtOAc/hexanes) provided 617 mg of N-(3-bromo-5-cyanophenyl)methanesulfonamide as a colorless solid in 88% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-425cd905b3054070853c4737dc9d49da
Source noteuspto-grants-2012_10