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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371047Generated: October 30, 2026

Thioacetamide → 2-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one

https://huagongshe.com/reaction/2371047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetamideHCID 2723949—
Reactant2-Bromocyclohexane-1,3-dioneHCID 2770476—
SolventEthanolHCID 702—
Product2-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-oneHCID 14913369—

Reaction Steps

To a solution of ethanethioamide (0.75 g, 10 mmol) in ethanol (20 mL) at room temperature was added 2-bromocyclohexane-1,3-dione (1.9 g, 10 mmol) in portions. The reaction solution was refluxed for 2 hours while stirring. After removal of solvents, the residue was diluted with water and washed with diethyl ether. The separated aqueous layer was basified with sodium carbonate solution. The resulting solid was collected by vacuum filtration, rinsed with water. The solid was suspended in methanol and followed by evaporation to dryness to produce the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710245B2
Source datasetuspto-grants-2014_04
ORD IDord-ce6dc72c650a4d18bcf495da9bdd852e
Source noteuspto-grants-2014_04