HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 104159-53-7
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Tris(dimethylamino)sulfanium trifluoromethanolate | HCID 22448444 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 104159-53-7 | HCID 13765566 | — |
Reaction Steps
α-Bromoacetophenone, 13.61 g (0.068 mol), was added dropwise at 25° to a solution of 0.076 mol of tris(dimethylamino)sulfonium trifluoromethoxide (prepared as in Example 1) in 75 mL of acetonitrile. The reaction mixture was stirred for 3 days and then poured into ice-water. The aqueous mixture was extracted with ether, and the ether extracts were washed with water, dried (MgSO4), and distilled to give α-trifluoromethoxyacetophenone as a colorless liquid: bp 64°-65° (0.8 mm); 1H NMR (CDCl3) δ5.15 ppm (s, 2H), 7.50 ppm (m, 3H), 7.85 ppm (m, 2H); 19F NMR (CDCl3) δ-61.5 ppm(s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04621125 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-a4ae467a9f2d4300a4fc5019deceb7a2 |
| Source note | uspto-grants-1986_11 |