Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833842Generated: November 1, 2026

Magnesium monoxide → 3-Benzylpyridazine

https://huagongshe.com/reaction/1833842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesium monoxideHCID 6850729—
ReactantHCID 15684248HCID 15684248—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-BenzylpyridazineHCID 59814993.8%

Reaction Steps

A solution of (±) 3-α-chlorobenzylpyridazine (2.05 g.) in ethanol (50 ml.) was treated with hydrogen, in the presence of magnesium oxide (0.4 g.) and palladium on charcoal (5% Pd; 0.2 g.), for 1 hour at ambient temperature and normal atmospheric pressure. The solution was then filtered and the filtrate was evaporated to dryness. The residue was dissolved in hot chloroform (100 ml.), cooled, washed with water (50 ml.), dried over magnesium sulphate and evaporated to give 3-benzylpyridazine (1.6 g.), m.p. 61°-64° C., in the form of a light brown coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067723
Source datasetuspto-grants-1978_01
ORD IDord-ab703a07c09346e8ab24ce79bed21700
Source noteuspto-grants-1978_01