HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 13765567, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | Tris(dimethylamino)sulfanium trifluoromethanolate | HCID 22448444 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13765567 | HCID 13765567 | — |
Reaction Steps
Bromodiphenylmethane, 20.7 g (0.084 mol), was added portionwise at 25° to a stirred solution of 0.093 mole of tris(dimethylamino)sulfonium trifluoromethoxide (prepared as in Example 1) in 75 mL of acetonitrile. The reaction mixture was stirred for 18 h and then poured into water. The aqueous mixture was extracted with ether, and the ether extracts were washed with water, dried (MgSO4), and then distilled to give 8.34 g of trifluoromethyl diphenylmethyl ether as a colorless oil: bp 83.3° (0.7 mm); 1H NMR (CDCl3) δ6.17 ppm (s, 1H), 7.27 ppm (m, 10H); 19F NMR (CDCl3) δ-58.4 ppm (s). Anal. Calcd. for C14H11F3O: C, 66.66; H, 4.40; F, 22.60. Found: C, 66.82; H, 4.57; F, 22.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04621125 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-ad29697e1081459a9c5d10578a020fec |
| Source note | uspto-grants-1986_11 |