HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222250Generated: October 30, 2026
Ethanol → tert-butyl 4-(3-phenyl-1H-pyrazol-5-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/222250
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | tert-Butyl 4-(3-oxo-3-phenylpropanoyl)piperidine-1-carboxylate | HCID 49760127 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl 4-(3-phenyl-1H-pyrazol-5-yl)piperidine-1-carboxylate | HCID 67109296 | — |
Reaction Steps
A mixture of tert-butyl 4-(3-oxo-3-phenylpropanoyl)piperidine-1-carboxylate (3.1 g), hydrazine monohydrate (0.5 mL), ethanol (30 mL), and THF (30 mL) was stirred at room temperature for about 15 hours, and at 60° C. for 1 hour. Hydrazine monohydrate (0.5 mL) was further added thereto, followed by stirring again at 60° C. for 3 hours. Hydrazine monohydrate (4.0 mL) was added thereto again, followed by stirring at 60° C. for 8 hours. After leaving to be cooled, the solvent was evaporated under reduced pressure, and to the residue were added diisopropyl ether and methanol, followed by stirring. The resulting solid was collected by filtration and dried under reduced pressure to obtain tert-butyl 4-(3-phenyl-1H-pyrazol-5-yl)piperidine-1-carboxylate (2.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207199B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-4edd8abd079f425ab29f50450bbf513d |
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| Source note | uspto-grants-2012_06 |
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