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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579274Generated: November 2, 2026

Epichlorohydrin → HCID 20360753, compound

https://huagongshe.com/reaction/1579274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPiperidineHCID 8082—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 19884680HCID 19884680—
SolventDichloromethaneHCID 6344—
ProductHCID 20360753HCID 2036075360.9%

Reaction Steps

A mixture of finely powdered 6-(3-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone (21.6 g, 0.11 mole), epichlorohydrin (90 ml, 1.1 mole), and piperidine (1ml) was heated on a steam bath for 90 minutes. Evaporation of the solution under reduced pressure gave an oil which was dissolved in dichloromethane and stirred with dilute sodium hydroxide solution (60 ml). The organic phase was washed with water, dried, and evaporated under reduced pressure to a viscous oil (27 g, 96%). Purification on a silica column by elution with chloroform gave 6-[3-(2,3-epoxypropoxy)phenyl]-4,5-dihydro-3(2H)-pyridazinone (16.5g, 59%) as an oil which when treated with ether gave a white solid (13.7g, 49%, m.p. 108°-112°C). The pure epoxide, recrystallised from methanol petroleum/ether (b.p. 60°-80°C), had m.p. 110°-112°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931177
Source datasetuspto-grants-1976_01
ORD IDord-6a8ad5c91fcf4f849a24c26d3bffb320
Source noteuspto-grants-1976_01