HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Phenyl-4-(4-trifluoromethylphenoxy)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzene, 1-fluoro-4-(trifluoromethyl)- | HCID 67873 | — |
| Reactant | 4-Phenylpiperidin-4-ol | HCID 96387 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Phenyl-4-(4-trifluoromethylphenoxy)piperidine | HCID 21268252 | 11.7% |
Reaction Steps
A mixture of 4-phenyl-4-piperidinol (7.1 g, 40 mM), DMSO (50 ml) and sodium hydride (2 g of a 50% dispersion in oil) was heated at 80° until homogenous, cooled to ambient temperature and treated with 4-fluorobenzotrifluoride (6.6 g, 40 mM) in DMSO (10 ml). After 24 hours the reaction mixture was poured on to cold water (250 ml) and extracted with ether (2×250 ml). The combined organic layers were washed with brine, dried and the solvent removed under reduced pressure. The residue was triturated with cyclohexane, filtered and the mother liquors evaporated and the residue triturated with pentane. Sublimation of the resulting crystals at 0.1 mm Hg (bath temp. 100°) gave the title compound (1.5 g), m.p. 104°-5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04325953 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-cd1fba3788f64c05976b042466f52790 |
| Source note | uspto-grants-1982_04 |