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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539956Generated: November 1, 2026

Acetic Anhydride → 1-(2,3-Dihydro-1,4-benzothiazepin-4(5H)-yl)ethanone

https://huagongshe.com/reaction/539956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepineHCID 12269106—
SolventDichloromethaneHCID 6344—
Product1-(2,3-Dihydro-1,4-benzothiazepin-4(5H)-yl)ethanoneHCID 14670716100%

Reaction Steps

To a solution of 2,3,4,5-tetrahydro-1,4-benzothiazepine (5 g, 30.3 mmol) in dry dichloromethane (100 mL) was added triethylamine (5.06 mL, 36.3 mmol) at room temperature, followed by the dropwise addition of acetic anhydride (3.43 mL, 36.3 mmol) at 0° C. under nitrogen. The resulting solution was stirred for 1 hour whilst allowing the temperature to rise slowly to room temperature. The mixture was washed with brine (50 mL×2), dried over sodium sulfate, filtered and concentrated in vacuo to afford 6.28 g of product as yellow oil, which was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-38763977d70f47ea9a4ea91a0bc82783
Source noteuspto-grants-2014_10