HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl- → 2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Cyclohexanedione, 2-bromo-5,5-dimethyl- | HCID 70958 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one | HCID 587874 | 83.7% |
Reaction Steps
28 g of 2-bromo-5,5-dimethylcyclohexane-1,3-dione and 11.7 g of thiourea are dissolved in 200 ml of ethanol. After the weakly exothermic reaction has subsided, the mixture is refluxed for a further 6 hours. The solution is diluted with 400 ml of water and neutralised with saturated sodium bicarbonate solution. The precipitated crystals are collected by filtration and dried in vacuo at 80° C., affording 21 g of 2-amino-5,5-dimethyl-7-oxo-4,5-dihydro-6H-benzthiazole with a melting point of 203°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04380640 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-1107443d59d84ce4ab9c5456efada9c3 |
| Source note | uspto-grants-1983_04 |