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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222244Generated: October 26, 2026

Hydrazine hydrate (1:1) → tert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/222244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1-tert-Butyl 4-ethylpiperidine-1,4-dicarboxylateHCID 26339893—
SolventEthanolHCID 702—
Producttert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—

Reaction Steps

A mixture of 1-tert-butyl 4-ethylpiperidine-1,4-dicarboxylate (21 g), hydrazine monohydrate (40 mL), and ethanol (200 mL) was heated and refluxed for 22 hours. After leaving to be cooled, the solvent was evaporated under reduced pressure, to the residue were added saturated brine and ethyl acetate, and the organic phase was separated. The organic phase was dried over magnesium sulfate and the solvent was evaporated under reduced pressure. To the residue was added diisopropyl ether, followed by stirring for 1 hour, and the resulting solid was collected by filtration and dried under reduced pressure to obtain tert-butyl 4-(hydrazinocarbonyl)piperidine-1-carboxylate (17.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207199B2
Source datasetuspto-grants-2012_06
ORD IDord-3e590f2b72cd459e8fe8cb50eb4cd178
Source noteuspto-grants-2012_06