HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl- → HCID 3123575, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl- | HCID 70958 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methylthiourea | HCID 2723704 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 3123575 | HCID 3123575 | 81.3% |
Reaction Steps
82 g of 2-bromo-5,5-dimethylcyclohexane-1,3-dione, 40 g of sodium acetate and 50 g of N-methylthiourea are dissolved in 500 ml of acetic acid. The mixture is stirred at room temperature until the weakly exothermic reaction has subsided, and then refluxed for 3 hours. The reaction mixture is then concentrated to one third of its volume in a rotary evaporator, poured into 100 ml of water and cooled to 0° C. The precipitate is collected by filtration and dried in vacuo at 80° C., affording 64 g of 2-methylamino-5,5-dimethyl-7-oxo-4,5-dihydro-6H-benzthiazole with a melting point of 217°-218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04380640 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-aa00dd27246240d9a70a7ba0ce1cd3d7 |
| Source note | uspto-grants-1983_04 |