HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methyl 2-bromo-2-(4-fluorophenyl)acetate | HCID 12717580 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-one | HCID 13690761 | 87.6% |
Reaction Steps
To a suspension of 2-aminothiophenol (12.6 g) and sodium acetate (23.6 g) in ethanol (150 ml) is added methyl α-bromo-4-fluorophenylacetate (23.6 g), and the mixture is stirred at room temperature overnight. After the solvent is distilled off, water is added to the residue. The resulting precipitate is separated by filtration, washed, dried, and then recrystallized from tetrahydrofuran-n-hexane to give 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (21.7 g) as crystals. M.p. 216°-219° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246929 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-c9f7e092e3be4773aba7a95c56f0342d |
| Source note | uspto-grants-1993_09 |