HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → BENZYL TRIFLUOROMETHYL SULFIDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 10236270 | HCID 10236270 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | BENZYL TRIFLUOROMETHYL SULFIDE | HCID 3782775 | 82% |
Reaction Steps
Benzyl bromide, 16.2 g (0.095 mol), was added dropwise at 25° to 0.11 mol of tris(dimethylamino)sulfonium trifluoromethanethiolate (prepared as in Example 11) in 75 mL of acetonitrile. The reaction mixture was stirred one h and then poured into water. The aqueous mixture was extracted with ether, and the ether extracts were washed with water, dried (MgSO4), and distilled to give 15.1 g (82%) of benzyl trifluoromethyl sulfide as a colorless liquid: bp 55° (12 mm); 1H NMR (CDCl3) δ4.08 ppm (s, 2H), 7.33 ppm (s, 5H); 19F NMR (CDCl3) δ-42.5 ppm (s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04621125 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-4c87adfe797146c79e5ed8511dfcb1b7 |
| Source note | uspto-grants-1986_11 |