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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734035Generated: October 31, 2026

4-Chlorobutyryl chloride → 7-(4-chlorobutyryl)-2,3-dihydrothieno[3,2-f][1,4]thiazepin-5(4H)-one

https://huagongshe.com/reaction/1734035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant3,4-dihydrothieno[3,2-f][1,4]thiazepin-5(2H)-oneHCID 4365942—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1-DichloroethaneHCID 6365—
Product7-(4-chlorobutyryl)-2,3-dihydrothieno[3,2-f][1,4]thiazepin-5(4H)-oneHCID 2147205659%

Reaction Steps

To a mixture of 13 g of 2,3-dihydrothieno[3,2-f][1,4]thiazepin-5(4H)-one and 21.5 g of 4-chlorobutyryl chloride in 200 ml of dichloroethane was added 21.5 g of aluminum chloride under cooling and the mixture was stirred for 3 hours. The mixture was poured into ice-cold water and extracted with chloroform. The organic layer was washed with saline solution, dried over magnesium sulfate and concentrated. The residue was recrystallized from ethanol to give 12 g of 7-(4-chlorobutyryl)-2,3-dihydrothieno[3,2-f][1,4]thiazepin-5(4H)-one as white crystals, m.p. 124°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532240
Source datasetuspto-grants-1996_07
ORD IDord-1e13a71674284da2bf458f42cd064284
Source noteuspto-grants-1996_07