HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 21450252, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21450220 | HCID 21450220 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21450252 | HCID 21450252 | 81.1% |
Reaction Steps
A mixture of finely ground 3-(4-hydroxybenzoyl)-N-methylpropionamide (20.7 g, 0.1 mole), epichlorohydrin (77 g, 0.83 mole), and piperidine (0.5 ml) was heated on a steam bath for 90 minutes. Evaporation under reduced pressure gave a viscous oil which was dissolved in dichloromethane (500 ml) and shaken with dilute sodium hydroxide (100 ml). The organic phase was washed with water, dried and evaporated to a slurry. Addition of ether gave the required 3-[4-(2,3-epoxypropoxy)benzoyl]-N-methylpropionamide (21.36g.,81%) which was recrystallised from chloroform/ether, m.p. 133°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04011321 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-0ca1b70f6b664cb1bd1203c2612d1269 |
| Source note | uspto-grants-1977_03 |