HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 21450254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(3-allyl-4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone | HCID 135573283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21450254 | HCID 21450254 | 47.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931177 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-db0ffb8a2cbb44e197bc2a5b54fc9645 |
| Source note | uspto-grants-1976_01 |