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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079338Generated: October 31, 2026

Ethanesulfonyl chloride → 4-Ethylsulphonyl-2,3,4,5-tetrahydro-1,4-benzothiazepine

https://huagongshe.com/reaction/1079338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepineHCID 12269106—
SolventDichloromethaneHCID 6344—
Product4-Ethylsulphonyl-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 9881574—

Reaction Steps

A solution of ethanesulphonyl chloride (3.8 g) in dichloromethane (50 ml) was added dropwise at room temperature to a stirred solution of 2,3,4,5-tetrahydro-1,4-benzothiazepine (4.29 g, prepared as described in the first paragraph of Example 6 above) in dichloromethane (100 ml). The reaction mixture was stirred at room temperature for one hour, washed with water, dried and the solvent was removed by evaporation. Purification of the residue by flash chromatography using trichloromethane as eluent gave 4-ethylsulphonyl-2,3,4,5-tetrahydro-1,4-benzothiazepine, which was recrystallised from hexane. Yield 4.25 g (m.p. 78°-80° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580866
Source datasetuspto-grants-1996_12
ORD IDord-1296b15049f148c2a3068159c381ea79
Source noteuspto-grants-1996_12