HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596685Generated: October 30, 2026
Epichlorohydrin → HCID 20360753, compound
https://huagongshe.com/reaction/596685
Participants
| Role | Name | HCID | Charge |
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| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19884680 | HCID 19884680 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20360753 | HCID 20360753 | 60.9% |
Reaction Steps
A mixture of finely powdered 6-(3-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone (21.6g, 0.11mole), epichlorohydrin (90ml, 1.1 mole), and piperidine (1 ml) 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 (27g, 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. (Found: C, 63.96; H, 5.70; N, 11.43: M+, 246. C13H 14 N2O3 requires: C, 63.39; H, 5.73; N, 11.38%. M, 246).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011321 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-37efc84f040c40b497f16b84b2c4abb9 |
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| Source note | uspto-grants-1977_03 |
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