HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-Methyl-2,3-dihydro-1H-phenothiazin-4(10H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | HCID 19602601 | HCID 19602601 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Methyl-2,3-dihydro-1H-phenothiazin-4(10H)-one | HCID 15621528 | — |
Reaction Steps
A mixture of ter butyl 6-methyl-2,4-dioxocyclohexane-1-carboxylate, 7c (3.09 g, 13.7 mmole) and 2-aminothiophenol, 6 (X=H, 1.71 g, 13.7 mmole) in DMSO (10 mL) is placed in a preheated heating mantle. The reaction mixture is stirred and refluxed for 0.5 h. Upon cooling, the reaction mixture forms a solid. The crystals are filtered and the remaining mother liquid is poured into cold water, whereupon further precipitation occurs. Each precipitate was separately recrystallized twice from MeOH and proves to be identical. An analytical sample of 4d, (R=H), mp 278° C. occurs as light orange crystals; yield: 0.46 g (15.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994349 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-c53f69dc79354be285c8875f7892502c |
| Source note | uspto-grants-1999_11 |