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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579271Generated: October 31, 2026

Epichlorohydrin → HCID 21450254, compound

https://huagongshe.com/reaction/1579271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPiperidineHCID 8082—
ReactantSodium HydroxideHCID 14798—
Reactant6-(3-allyl-4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinoneHCID 135573283—
SolventDichloromethaneHCID 6344—
ProductHCID 21450254HCID 2145025447.6%

Reaction Steps

A mixture of finely ground 6-(3-allyl-4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone (50 g, 0.22 mole), epichlorohydrin (200 g, 2.2 mole) and piperidine (2 g) was heated on a steam bath for 90 minutes. Evaporation under reduced pressure gave a viscous oil which was dissolved in dichloromethane and stirred for 10 minutes with dilute sodium hydroxide (500 ml). The organic phase was washed with water, dried and evaporated to an oil which slowly solidified. Addition of ethanolether gave 6-[3-allyl-4-(2,3-epoxypropoxy)phenyl]-4,5-dihydro-3(2H)-pyridazinone (30 g, 47%, m.p. 92.5°-95°C) which was recrystallised from aqueous ethanol to give the pure pyridazinone (m.p. 93.5°-95°C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931177
Source datasetuspto-grants-1976_01
ORD IDord-db0ffb8a2cbb44e197bc2a5b54fc9645
Source noteuspto-grants-1976_01