Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Nitrourea | HCID 62372 | — |
| Reactant | 4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidine | HCID 14649978 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14649979 | HCID 14649979 | 64.81% |
Reaction Steps
A mixture of 4.89 g of 4-(2,3,4,5,6-pentafluorophenoxy)-4-phenylpiperidine, 50 ml of 95% ethanol and 2.1 g of nitrourea was refluxed at 70° C. until the evolution of gas had ceased. After refluxing for an additional 30 minutes, the mixture was cooled, treated with 200 ml of water and extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated. The concentrate was purified by means of high pressure liquid chromatography (silica gel; elution with ethyl acetate) to yield 3.5 g (64.81%) of 1-aminocarbonyl-4-(2,3,4,5,6-pentafluorophenoxy)-4-phenylpiperidine, m.p. 155°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853384 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-4ce835f9cd4d47babdc781b5a6f611fb |
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| Source note | uspto-grants-1989_08 |
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