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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776477Generated: November 1, 2026

Methanesulfonyl chloride → HCID 86679430, compound

https://huagongshe.com/reaction/1776477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(Cyclopropylmethoxy)anilineHCID 19626923—
SolventPyridineHCID 1049—
ProductHCID 86679430HCID 8667943096%

Reaction Steps

A solution of 2-(cyclopropylmethoxy)aniline (1.03 g, 6.31 mmol) in pyridine (20 ml) was cooled to 0° C., and methanesulfonyl chloride (0.541 ml, 6.94 mmol) was added. The mixture was warmed to RT and stirred for 2 hours. The solvent was removed, and the crude was portioned between EtOAc and HCl 1N. The organic phase was washed with brine and dried over Na2SO4. The solvent was removed and the crude was purified by filtration on silica gel cartridge (petroleum ether:EtOAc=80:20) affording N-(2-(cyclopropylmethoxy)phenyl)methanesulfonamide (1.456 g, 6.03 mmol, 96% yield, MS/ESI+ 263.9 [MNa]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-77fa96ab6cbb42be897c6d7004b76095
Source noteuspto-grants-2016_02