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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539954Generated: November 3, 2026

Potassium Hydroxide → 5-Methyl-2,3-dihydro-1,4-benzothiazepine

https://huagongshe.com/reaction/539954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Bromoethylamine hydrobromideHCID 2774217—
Reactant1-(2-Sulfanylphenyl)ethan-1-oneHCID 11094819—
SolventEthanolHCID 702—
Product5-Methyl-2,3-dihydro-1,4-benzothiazepineHCID 2007229779.4%

Reaction Steps

To a solution of 1-(2-sulfanylphenyl)ethanone (6.40 g, 42.05 mmol) in ethanol (80 mL) was added an aqueous solution of potassium hydroxide (7.08 g, 126.14 mmol in 30 mL of water) and an aqueous solution of 2-bromoethanamine hydrobromide (9.48 g, 46.25 mmol in 30 mL of water). After being stirred at room temperature for 6 hours, the reaction mixture was concentrated in vacuo to remove most of ethanol and extracted with dichloromethane (60 mL×3). The combined organic layers were washed with brine (100 mL), dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by flash column chromatography to give 5.92 g of 5-methyl-2,3-dihydro-1,4-benzothiazepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-0184d1ea78ce40eaa972cb24ba19dc1e
Source noteuspto-grants-2014_10