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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085131Generated: November 1, 2026

Ethanesulfonyl chloride → HCID 20061013, compound

https://huagongshe.com/reaction/1085131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantHCID 20061015HCID 20061015—
SolventPyridineHCID 1049—
ProductHCID 20061013HCID 20061013—

Reaction Steps

A suspension of the aniline from example 14 (0.5 g, 1.3 mmol) in dry pyridine (3 ml) was treated with ethanesulphonyl chloride (0.133 ml, 1.4 mmol). After 1 h, the mixture was evaporated to dryness then partitioned between dichloromethane and dilute aqueous sodium bicarbonate. The organic phase was dried over magnesium sulphate and evaporated to a yellow solid which was recrystallised from ethyl acetate (0.37 g, 59%). M.p. 258°-260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008263
Source datasetuspto-grants-1991_04
ORD IDord-cc3fbe84a8cb49f3af797ed6600be5b1
Source noteuspto-grants-1991_04