HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → 6-Methyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Bromo-4-methylcyclohexan-1-one | HCID 12490455 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Methyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04321372 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-6c21d931920e406a87f2ad2e4e7c0c6d |
| Source note | uspto-grants-1982_03 |