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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222245Generated: October 30, 2026

HCID 58270830, compound → HCID 67108946, compound

https://huagongshe.com/reaction/222245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58270830HCID 58270830—
SolventPhosphorus oxychlorideHCID 24813—
ProductHCID 67108946HCID 6710894635%

Reaction Conditions

Temperature80 °C

Reaction Steps

To benzyl 4-{[2-(4-fluorophenyl)-2-oxoethyl]carbamoyl}piperidine-1-carboxylate (5.5 g) was added phosphorous oxychloride (20 mL), followed by stirring at 80° C. for 3 hours. After leaving to be cooled, the reaction liquid was concentrated under reduced pressure, and the residue was azeotroped with toluene three times. To the residue were added ethyl acetate and water, and the organic phase was separated. The organic phase was washed with a saturated aqueous sodium bicarbonate and saturated brine in this order, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=70/30 to 30/70) to obtain benzyl 4-[5-(4-fluorophenyl)-1,3-oxazol-2-yl]piperidine-1-carboxylate (1.84 g) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207199B2
Source datasetuspto-grants-2012_06
ORD IDord-8476ebb182d048a2addd1062affb350e
Source noteuspto-grants-2012_06