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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38225Generated: October 26, 2026

Methanesulfonyl chloride → N-(3-ethynylphenyl)methanesulfonamide

https://huagongshe.com/reaction/38225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
SolventPyridineHCID 1049—
ProductN-(3-ethynylphenyl)methanesulfonamideHCID 57131399—

Reaction Steps

To a solution of 3-ethynyl aniline (1.05 mL, 10.0 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (857 μL, 1.10 eq.) at a temperature of 0° C. The resulting mixture was stirred overnight at room temperature and was then evaporated. The residue was treated with 2 N aq. HCl (25 mL) and subsequently extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over MgSO4 and evaporated to give the desired methanesulfonamide in quantitative yield. It was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524724B2
Source datasetuspto-grants-2013_09
ORD IDord-e04eb91ca7634a4a97f9b40e63bc61d3
Source noteuspto-grants-2013_09