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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753786Generated: October 28, 2026

Potassium Hydroxide → (6-Hydrazinopyridin-3-yl)methanol

https://huagongshe.com/reaction/1753786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(6-Chloropyridin-3-yl)methanolHCID 177161—
Product(6-Hydrazinopyridin-3-yl)methanolHCID 59186956—

Reaction Conditions

Temperature150 °C

Reaction Steps

220.0 g (1.5 mol) (6-chloropyridin-3-yl)methanol [Evans et al., Organic Letters 2001, 19, 3009-3012] are initially introduced into 746 ml (767.1 g, 15.3 mol) hydrazine hydrate and the mixture is stirred at a bath temperature of 150° C. for 5 h. The reaction mixture is concentrated in vacuo, the residue is taken up in 500 ml water and 86.0 g (1.5 mol) potassium hydroxide are added. The mixture is stirred for 15 min, the water is then removed almost completely on a rotary evaporator and the residues of water are distilled off azeotropically with toluene several times. The oily residue is stirred in ethanol, the mixture is cooled to approx. 10° C., the potassium chloride which has precipitated out is filtered off, the filtrate is concentrated, diethyl ether is added to the residue and the mixture is stirred. Finally, the product is filtered off, the residue on the filter is washed with diethyl ether and the crystals are dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09168249B2
Source datasetuspto-grants-2015_10
ORD IDord-da87c25d339c44b7a01ea7b22ad82e93
Source noteuspto-grants-2015_10