Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantNitroureaHCID 62372—
Reactant4-(2,3,4,5,6-Pentafluorophenoxy)piperidineHCID 14837040—
SolventEthanolHCID 702—
Product1-Aminocarbonyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 1976246273.4%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212184
Source datasetuspto-grants-1993_05
ORD IDord-9d6390a6c1ee4c4f86c013f205aa450a
Source noteuspto-grants-1993_05