Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651738Generated: November 2, 2026

Epichlorohydrin → HCID 20059095, compound

https://huagongshe.com/reaction/1651738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant2-Furanmethanol, 5-(dimethoxymethyl)-HCID 588127—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 20059095HCID 20059095—

Reaction Steps

5-Glycidoxymethyl furfuraldehyde dimethyl acetal was prepared by adding a total of 6.0 g (0.035 mole) of 5-hydroxymethyl furfuraldehyde dimethyl acetal (HMFA) to 1.54 g sodium hydroxide (0.038 mole) in a 100 ml round bottom flask equipped with magnetic stir bar, reflux condenser, and nitrogen inlet. After stirring for 30 min., 3.89 g (0.042 mole) of epichlorohydrin in 50 ml. of methyl ethyl ketone was added quickly, and the reaction mixture was allowed to reflux overnight under an inert (nitrogen) atmosphere. The mixture was then cooled, filtered, and the solvent removed under vacuum. The resulting oil was mixed with 250 ml of toluene and the toluene was distilled off at atmospheric pressure to remove any residual epichlorohydrin. The sample was freed of toluene by subjecting it to high vacuum overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929670
Source datasetuspto-grants-1990_05
ORD IDord-337038d7fbad4d40955c082208081be3
Source noteuspto-grants-1990_05