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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596681Generated: November 1, 2026

Epichlorohydrin → HCID 21450254, compound

https://huagongshe.com/reaction/596681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant3-(2-Hydroxybenzoyl)propionic acidHCID 3016086—
Reactant6-(3-allyl-4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinoneHCID 135573283—
SolventDichloromethaneHCID 6344—
ProductHCID 21450254HCID 2145025447%

Reaction Steps

A mixture of finely ground 6-(3-allyl-4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone (50g, 0.22 mole), epichlorohydrin (200 g, 2.2 mole) and piperidine (2g) 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 ethanol-ether gave 6[3-allyl-4-(2,3-epoxypropoxy)phenyl]-4,5-dihydro-3(2H)-pyridazinone (30g, 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 numberUS04011321
Source datasetuspto-grants-1977_03
ORD IDord-a2da714099554429bb63ad349a11e8a3
Source noteuspto-grants-1977_03