HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248869Generated: October 26, 2026
Water → 1-Aminocarbonyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine
https://huagongshe.com/reaction/248869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Nitrourea | HCID 62372 | — |
| Reactant | 4-(2,3,4,5,6-Pentafluorophenoxy)piperidine | HCID 14837040 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Aminocarbonyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine | HCID 19762462 | 73.4% |
Reaction Steps
A solution of 4.0 g of 4-(2,3,4,5,6-pentafluorophenoxy)piperidine in 100 ml of 95% ethanol was treated with 1.73 g of nitrourea and then stirred at 65° C. for five hours. After cooling to room temperature, the reaction mixture was poured into water 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. Filtration, followed by evaporation of the solvents afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 5% methanol/dichloromethane). The resultant solid was recrystallized from hot isopropanol to yield 3.41 g (73.3%) of 1-aminocarbonyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine, m.p. 170°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212184 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-9d6390a6c1ee4c4f86c013f205aa450a |
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| Source note | uspto-grants-1993_05 |
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