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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464442Generated: October 31, 2026

Methanesulfonyl chloride → HCID 15293135, compound

https://huagongshe.com/reaction/1464442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15293134HCID 15293134—
SolventPyridineHCID 1049—
ProductHCID 15293135HCID 15293135—

Reaction Steps

To a stirred solution of the title compound of Example 13 (1.0 g) in pyridine (15 mL) under nitrogen at approximately 5° C. (ice water bath) was added dropwise via syringe methanesulfonyl chloride (0.28 mL). The ice bath was removed, and the reaction was stirred at ambient temperature for 2 hours. The reaction was then evaporated under vacuum, and the residue was treated with 1 M HCl. The insoluble product was collected by filtration, washed twice with 1 M HCl, and then with water. The solid was suspended in methanol, heated to reflux on a steam bath, cooled to room temperature, and the product was collected by filtration. Recrystallization from acetonitrile yielded the title compound as a pinkish solid. Mp: 211°-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304644
Source datasetuspto-grants-1994_04
ORD IDord-a9e27ee0aa9a4d6ca9fd13a2d1f3a841
Source noteuspto-grants-1994_04