HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinone → Phenothiazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinone | HCID 4650 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Phenothiazone | HCID 68485 | 62.7% |
Reaction Steps
To a stirring suspension of 1.72 kg (16 mol) of p-benzoquinone in 13 liters MeOH at room temperature was added slowly a solution of 1.0 kg (8 mol) of 2-aminothiophenol in 600 ml MeOH over a period of 1 hour. The resulting red mixture was stirred at room temperature for another 2 hours and then the product 3H-phenothiaz-3-one was filtered off. This 3H-phenothiazin-3-one was washed thoroughly with methanol and dried to give 1.07 kg of 3H-phenothiazin-3-one (61.49% yield), m.p. 157°-159° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04667032 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-039689e1c73543b8aeaf486cf288a1b9 |
| Source note | uspto-grants-1987_05 |