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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913183Generated: October 31, 2026

Hydrazine hydrate (1:1) → Tert-butyl 6-hydrazinylpyridine-3-carboxylate

https://huagongshe.com/reaction/1913183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantTert-butyl 6-chloropyridine-3-carboxylateHCID 11521348—
SolventEthanolHCID 702—
ProductTert-butyl 6-hydrazinylpyridine-3-carboxylateHCID 45089857—

Reaction Conditions

Temperature100 °C

Reaction Steps

18.0 g (84.2 mmol) of tert-butyl 6-chloropyridine-3-carboxylate are initially charged in 85 ml of ethanol. 42.2 g (842.0 mmol) of hydrazine hydrate are added, and the mixture is stirred at 100° C. for 2 h. The mixture is then concentrated, and the residue is taken up in a mixture of ethyl acetate and water. The phases are separated, and the organic phase is washed once with water and once with saturated sodium chloride solution, dried over magnesium sulfate and concentrated again. The residue is triturated with petroleum ether, and the solid formed is filtered off and dried under high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609698B2
Source datasetuspto-grants-2013_12
ORD IDord-414f3b0fdf38488f9e140f7c9557fa4f
Source noteuspto-grants-2013_12