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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833858Generated: November 4, 2026

Methanol → Sodium Methoxide

https://huagongshe.com/reaction/1833858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21387569HCID 21387569—
ProductSodium MethoxideHCID 10942334—
ProductHCID 15684250HCID 15684250—

Reaction Steps

A solution of sodium methoxide was prepared by the addition of sodium hydride (0.72 g.) to methanol (25 ml.). (±) 3-α-Chlorobenzylpyridazine (prepared as described in Example 2) (4.1 g.) was heated at reflux in this solution for 2 hours and the mixture was evaporated to dryness. The residue was dissolved in a mixture of diethyl ether and water and the ethereal layer was separated, dried over sodium sulphate and evaporated to give a brown oil. Distillation of this oil gave (±) 3-α-methoxybenzylpyridazine (1.8 g.), b.p. 140°-180° C./0.2-0.4 mm.Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067723
Source datasetuspto-grants-1978_01
ORD IDord-f4cea04706ea45b78a789c209f2a33a4
Source noteuspto-grants-1978_01