Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Methanethioamide | HCID 3005587 | — |
| Reactant | HCID 22313787 | HCID 22313787 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22313804 | HCID 22313804 | 86% |
Reaction Steps
To a stirred solution of phosphorus pentasulfide (4.0 g, 9.0 mmol) in dioxane (40 ml) was added formamide (4.8 g, 106 mmol), and the mixture was heated at reflux temperature for 2 hours. The reaction mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2-bromo-1-(2-fluoro-4-hydroxyphenyl)-1-ethanone (1.2 g, 5.15 mmol) in dioxane (14 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 2N NaOH aqueous solution. The whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-exane (1:4) to give title compound (864 mg, 86% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06603008B1 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-422ff8565f94414eb98611edfbe6c8bc |
|---|
| Source note | uspto-grants-2003_08 |
|---|