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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486471Generated: October 29, 2026

Methanol → R 61837

https://huagongshe.com/reaction/486471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 15124568HCID 15124568—
SolventWaterHCID 962—
ProductR 61837HCID 12750450%

Reaction Steps

To a stirred sodium methoxide solution, previously prepared starting from 1.6 parts of sodium in 24 parts of methanol, were added 4 parts of 3-chloro-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine. The whole was stirred and refluxed for 40 hours. After cooling 25 parts of water were added. The product was filtered off, washed with water and dissolved in trichloromethane. The organic layer was dried, filtered and evaporated. The residue was crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product was filtered off and dried, yielding 2 parts (50%) of 3-methoxy-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine; mp. 137.1° C. (compound 258).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-b37c733004fb47d69e99b4a7c5fadde4
Source noteuspto-grants-1994_03