HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2,4-di-t-butyl-1-hydroxy-10H-phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | 3,5-Di-tert-butyl-1,2-benzoquinone | HCID 76915 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,4-di-t-butyl-1-hydroxy-10H-phenothiazine | HCID 13882035 | — |
Reaction Steps
To a solution of 3,5-di-t-butyl-1,2-benzoquinone (2.2 q) in methanol (15 ml) cooled in an ice bath was added 2-aminothiophenol (1.38 g) and the mixture was stirred for 2 hours. A solid precipitate was filtered off and crystallized from heptane to yield the title compound m.p. 202°-212° (dec.). From the methanol filtrate there was obtained, after chromatography and crystallization, an additional crop of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845083 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-03b6e877bf1b4ebcb605976dc3437dd0 |
| Source note | uspto-grants-1989_07 |