HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031545Generated: October 23, 2026
Water → 4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidine
https://huagongshe.com/en/reaction/1031545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hexafluorobenzene | HCID 9805 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Phenylpiperidin-4-ol | HCID 96387 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidine | HCID 14649978 | 44% |
Reaction Steps
To a suspension of sodium hydride (60% in oil, 6.4 g) in 50 ml of dry dimethylformamide was added, over a period of ten minutes, a solution of 25 g of 4-hydroxy-4-phenylpiperidine in 100 ml of dry dimethylformamide. After stirring at 50° C., for thirty minutes, the reaction mixture was cooled to ice bath temperature (5° C.). A solution of 18.6 ml of hexafluorobenzene in 100 ml of dry dimethylformamide was then added over a period of thirty minutes, and the resulting mixture stirred at ambient temperature for twenty hours. The mixture was poured into 500 ml water, stirred for five minutes, and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, evaporation of the solvents afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 20% methanol/dichloromethane) to afford 21 g (44%) of 4-(2,3,4,5,6-pentafluorophenoxy)-4-phenylpiperidine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04954511 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-328e9c6847e348d78475cd9183d1ee0d |
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| Source note | uspto-grants-1990_09 |
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