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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596667Generated: October 31, 2026

Epichlorohydrin → HCID 21450252, compound

https://huagongshe.com/reaction/596667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPiperidineHCID 8082—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21450220HCID 21450220—
SolventDichloromethaneHCID 6344—
ProductHCID 21450252HCID 2145025281.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011321
Source datasetuspto-grants-1977_03
ORD IDord-0ca1b70f6b664cb1bd1203c2612d1269
Source noteuspto-grants-1977_03