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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285347Generated: October 30, 2026

Acetic Anhydride → HCID 70453272, compound

https://huagongshe.com/reaction/1285347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 70510120HCID 70510120—
SolventAcetic AcidHCID 176—
ProductHCID 70453272HCID 70453272—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1 g of (±)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride, 2 ml of acetic anhydride and 2 ml of acetic acid is stirred at 110° C. for 4 hours. Then, the reaction mixture is evaporated under reduced pressure to remove solvent. Ether is added to the residue, and the precipitated crystals are collected by filtration. 1.08 g of (±)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride are thereby obtained. Recrystallization of the product from a mixture of chloroform, ethanol and ether gives crystals (needles) melting at 159°-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567175
Source datasetuspto-grants-1986_01
ORD IDord-2e919370d0514681af72c645cbf41341
Source noteuspto-grants-1986_01