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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526439Generated: October 29, 2026

Hydrazine hydrate (1:1) → 1-(5-Bromo-4-methylpyridin-2-YL)hydrazine

https://huagongshe.com/reaction/526439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant5-Bromo-2-chloro-4-methylpyridineHCID 2734427—
SolventEthanolHCID 702—
Product1-(5-Bromo-4-methylpyridin-2-YL)hydrazineHCID 5340298553%

Reaction Conditions

Temperature120 °C

Reaction Steps

Combined 5-bromo-2-chloro-4-methylpyridine (15.0 g, 72.46 mmol) and EtOH (60 mL) and added hydrazine hydrate (85%, 45 mL) and stirred at 120° C. overnight. The reaction mixture was concentrated to give a residue which was extracted with EtOAc (50 mL×2) and water (50 mL×2). Then combined organic layers were extracted with brine, dried over Na2SO4 to and concentrated to give a residue which was purified by flash chromatography (petroleum ether: EtOAc=10:1 to 1:5) to give the title compound (7.8 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345713B2
Source datasetuspto-grants-2016_05
ORD IDord-b607b20b44504d0c9ea7dd17e0e16a6d
Source noteuspto-grants-2016_05