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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36569Generated: October 30, 2026

Water → 4-Acryloyl-2-[4-methoxyphenyl]-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine

https://huagongshe.com/reaction/36569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAnisoleHCID 7519—
Reactant4-Acryloyl-2-chloro-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 15291647—
SolventDichloromethaneHCID 6344—
Product4-Acryloyl-2-[4-methoxyphenyl]-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 1529164859%

Reaction Steps

The above-mentioned 4-acryloyl-2-chloro-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (2.3 g) and anisole (1.1 g) were dissolved in methylene chloride (50 ml) and stannic chloride (2.8 g) was added thereto and agitated at room temperature for 2 hours. To the reaction mixture water was added and extracted with chloroform. The chloroform phase was washed with a saturated saline solution and dried on sodium sulfate and thereafter the solvent was distilled out under reduced pressure. Residue was purified by silica gel column chromatography (Wako Gel C-200, 50 g) and eluted with a mixed solvent of n-hexane (70 parts)+ethyl acetate (30 parts) to give 4-acryloyl-2-[4-methoxyphenyl]-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416066
Source datasetuspto-grants-1995_05
ORD IDord-4a411b1b7007494db70c36a9bc8ed7aa
Source noteuspto-grants-1995_05