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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079325Generated: October 27, 2026

m-Chloroperbenzoic acid → 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide

https://huagongshe.com/reaction/1079325

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 9837680—
SolventDichloromethaneHCID 6344—
Product4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxideHCID 10220764—

Reaction Steps

A solution of 3-chloroperbenzoic acid (1.14 g) in dichloromethane (100 ml) was added dropwise with cooling from 0° C. to -2° C. to a stirred solution of 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.34 g, prepared as Example 9 above) in dichloromethane (50 ml). The reaction mixture was stirred for 15 minutes, washed with water, dried and the solvent was removed by evaporation at reduced pressure. Purification of the residue by flash chromatography using dichloromethane/ethanol (95:5) as eluent gave 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide, which was recrystallised from ethyl acetate. Yield 1.15 g (m.p. 119°-121° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580866
Source datasetuspto-grants-1996_12
ORD IDord-3c268fbe2ed54558a799f9b25e0286dd
Source noteuspto-grants-1996_12