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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67560689 | HCID 67560689 | — |
| Solvent | Water | HCID 962 | — |
| Product | [1-Benzyl-4-(4-fluorophenyl)piperidine-4-carbonyl]-oxidoazanium | HCID 88283475 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05635510 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-4a5125ad5f404045b57a0b4428eeaafd |
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| Source note | uspto-grants-1997_06 |
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