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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280519Generated: October 29, 2026

Acetic Anhydride → HCID 86740807, compound

https://huagongshe.com/reaction/280519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 70483404HCID 70483404—
SolventAcetic AcidHCID 176—
ProductHCID 86740807HCID 86740807—

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 0.618 g of (±)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-6,7-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride, 6 ml of acetic anhydride and 6 ml of acetic acid is heated at 105° C. for 18 hours. After the reaction is completed, the mixture is evaporated under reduced pressure to remove solvent. Benzene is added to the residue, and the mixture is evaporated under reduced pressure to remove solvent. The residue is recystallized from a mixture of ethanol and ether. 0.44 g of (±)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-6,7-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride 3/2 H2O is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590188
Source datasetuspto-grants-1986_05
ORD IDord-38fd644dc1c4490d851bd0a413646e43
Source noteuspto-grants-1986_05