Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059050Generated: October 30, 2026

Thiourea → 6-Methyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine

https://huagongshe.com/reaction/2059050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant2-Bromo-4-methylcyclohexan-1-oneHCID 12490455—
SolventEthanolHCID 702—
Product6-Methyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amineHCID 346922—

Reaction Steps

Thiourea (22.3 g., 0.29 mole) was slurried in 275 ml. of ethanol. 2-Bromo-4-methylcyclohexanone was added and the mixture heated to reflux for 75 minutes. The reaction mixture was cooled to room temperature and the crude product recovered as the hydrobromide salt by filtration. The crude salt was dissolved in warm water, filtered and made basic with ammonium hydroxide to precipitate the free base as an oil, which crystallized on cooling. Purified 2-amino-4,5,6,7-tetrahydro-6-methylbenzthiazole (25.2 g., m.p. 98°-100° C.) was obtained by recrystallization from cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04321372
Source datasetuspto-grants-1982_03
ORD IDord-6c21d931920e406a87f2ad2e4e7c0c6d
Source noteuspto-grants-1982_03