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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978340Generated: October 30, 2026

Acetic Anhydride → HCID 70430585, compound

https://huagongshe.com/reaction/978340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 70461456HCID 70461456—
SolventAcetic AcidHCID 176—
ProductHCID 70430585HCID 7043058589.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 0.95 g of (±)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-9-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride hydrate, 10 ml of acetic anhydride and 10 ml of acetic acid is stirred at 110° C. for 6.5 hours. After the reaction is completed, the reaction mixture is evaporated under reduced pressure to remove solvent. Toluene is added to the residue, and the mixture is evaporated under reduced pressure to remove solvent. The residue is recrystallized from a mixture of methanol and ether. 0.93 g of (±)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-9-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride hydrate is obtained. Yield: 89.4%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665068
Source datasetuspto-grants-1987_05
ORD IDord-751eecfd4df44982890d44364f2582fc
Source noteuspto-grants-1987_05