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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749663Generated: October 31, 2026

Hydrazinecarboxaldehyde → HCID 178451807, compound

https://huagongshe.com/reaction/1749663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazinecarboxaldehydeHCID 12229—
ReactantTert-butyl 4-(ethoxy(imino)methyl)piperidine-1-carboxylateHCID 21098368—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178451807HCID 17845180792%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of tert-butyl 4-(ethoxy(imino)methyl)piperidine-1-carboxylate (51 g, 198.95 mmol) in dioxane (500 mL), was added formohydrazide (17.92 g, 298.43 mmol). This solution was left to stir at 40° C. overnight under N2 resulting in precipitation of a white solid (hydrazide intermediate). The reaction mixture was then heated to 80° C. for 6 h, cooled to room temperature and concentrated. The residue was dissolved in 500 mL of CH2Cl2 and 300 mL of water was added. The phases were decanted and the organic phase was washed with brine, dried over MgSO4, filtered and concentrated to afford tert-butyl 4-(1H-1,2,4-triazol-3-yl)piperidine-1-carboxylate (46.0 g, 92%) as a white solid: 1H NMR Spectrum; (CDCl3) 1.47 (9H, s), 1.76 (2H, m), 1.98-2.11 (2H, m), 2.91 (2H, s), 2.97-3.08 (m, 1H), 4.06-4.23 (2H, m), 8.05 (1H, s); Mass Spectrum [M+H]+=no mass ion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156831B2
Source datasetuspto-grants-2015_10
ORD IDord-6352c42abc6e40058b994d138b08fe43
Source noteuspto-grants-2015_10