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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910437Generated: November 1, 2026

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

https://huagongshe.com/reaction/1910437

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 addition of acetic anhydride (3.43 mL, 36.3 mmol) dropwise 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 numberUS08604019B2
Source datasetuspto-grants-2013_12
ORD IDord-385c5c827fcd4431925ff99cac654ca1
Source noteuspto-grants-2013_12