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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683121Generated: October 30, 2026

Ethanol → [1-Benzyl-4-(4-fluorophenyl)piperidine-4-carbonyl]-oxidoazanium

https://huagongshe.com/reaction/1683121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67560689HCID 67560689—
SolventWaterHCID 962—
Product[1-Benzyl-4-(4-fluorophenyl)piperidine-4-carbonyl]-oxidoazaniumHCID 88283475—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Benzyl-4-(4-fluoro-phenyl)-4-cyano-piperidine hydrochloride (7.8 g, 26.5 mmol) was combined with aqueous sodium hydroxide (1.2 mL, 50% by weight) and ethanol (130 mL) and the mixture was heated to 50° C. The heating was removed, and a solution of hydrogen peroxide (12.11 mL, 30% by weight in water, 106 mmol) was added at such a rate that the temperature of the reaction mixture does not rise above 50° C. The reaction mixture was then stirred at 50° C. for 4 hours. The reaction mixture was diluted with water (100 mL) and most of the solvent was removed in vacuo before adding water (200 mL) to form a solid which was collected by filtration, rinsed with water, and dried in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635510
Source datasetuspto-grants-1997_06
ORD IDord-4a5125ad5f404045b57a0b4428eeaafd
Source noteuspto-grants-1997_06