Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459699Generated: October 30, 2026

Epichlorohydrin → 2-[(3-Methylbutoxy)methyl]oxirane

https://huagongshe.com/reaction/459699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
ReactantIsoamyl AlcoholHCID 31260—
Catalyst4-Hydroxybenzenesulfonic acidHCID 4765—
CatalystAluminum isopropoxideHCID 11143—
SolventWaterHCID 962—
Product2-[(3-Methylbutoxy)methyl]oxiraneHCID 8593698%

Reaction Conditions

Temperature90 °C

Reaction Steps

3-Methylbutanol (158 g, 1.78 mol), aluminum triisopropoxide (3.61 g, 17.7 mmol) and p-phenolsulfonic acid (9.40 g, 54 mmol) were charged into a 1-liter reaction vessel and the whole was heated to 90° C. with stirring. After an additional. 1 hour of stirring under reduced pressure (266 hPa). The vessel was heated to 100° C. and epichlorohydrin (170 g, 1.78 mol) was added dropwise thereto over a period of 30 minutes, followed by an additional 3 hours of stirring. The reaction mixture was kept at a 50° C. and 50% sodium hydroxide aqueous solution (285 g, 3.56 mol) was added dropwise thereto over a period of 1 hour. After an additional 3 hours of stirring, 400 ml of water was added to the mixture and the mixture was allowed to separate into layers. After removal of the water layer, 100 ml of toluene was added to the oil layer and the resulting solution was washed with 300 ml of 5% brine three times and concentrated to obtain a crude reaction product (218 g). Distillation of the product gave 3-methylbutyl glycidyl ether (150 g) (bp: 63–64° C./5 hPa, yield 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196052B2
Source datasetuspto-grants-2007_03
ORD IDord-eb14a1bebd5143518523294f5d24fa33
Source noteuspto-grants-2007_03