Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715068Generated: October 31, 2026

Methanesulfonyl chloride → N-(6-benzenesulfonyl-naphthalen-1-ylmethyl)-methanesulfonamide

https://huagongshe.com/reaction/1715068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantC-(6-Benzenesulfonyl-naphthalen-1-yl)-methylamineHCID 59028770—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(6-benzenesulfonyl-naphthalen-1-ylmethyl)-methanesulfonamideHCID 59028783—

Reaction Steps

C-(6-Benzenesulfonyl-naphthalen-1-yl)-methylamine is dissolved in methylene chloride and pyridine, and the mixture is cooled in an ice bath. Methanesulfonyl chloride is added dropwise, and the reaction mixture is stirred at ice bath temperature, then allowed to warm to room temperature. The reaction mixture is quenched by addition of water and extracted with methylene chloride. The organic layer is washed with water, dried (MgSO4), filtered and concentrated under reduced pressure to give N-(6-benzenesulfonyl-naphthalen-1-ylmethyl)-methanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799797B2
Source datasetuspto-grants-2010_09
ORD IDord-e0871e27db9d427a91609cc1c2f50d69
Source noteuspto-grants-2010_09