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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792167Generated: October 31, 2026

Epichlorohydrin → HCID 15965804, compound

https://huagongshe.com/reaction/1792167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantHCID 23667177HCID 23667177—
CatalystTetramethylammonium chlorideHCID 6379—
SolventWaterHCID 962—
ProductHCID 15965804HCID 15965804—

Reaction Conditions

Temperature120 °C

Reaction Steps

Into a 200 mL three-necked flask equipped with a stirrer and reflux tube was charged 37.83 g (0.3 mol) of sodium 2-hydroxyisobutyrate, 138.7 g (1.5 mol) of epichlorohydrin, 0.25 g of tetramethylammonium chloride and pure water at room temperature under normal pressure, and heated at temperatures from room temperature to an inner temperature of 120° C. over a period of 10 minutes, then, reacted while keeping this temperature for 1.5 hours, then, cooled to room temperature. To this was added water and allowed to stand for 1.5 hours, then, an organic solvent phase was removed. After epichlorohydrin was distilled off in a distillation apparatus equipped with a Vigreux distilling column, the obtained residual liquid was distilled under reduced pressure to obtain glycidyl 2-hydroxyisobutyrate. The charging molar ratio, reaction conditions and reaction yield, and the amount of by-products after distillation under reduced pressure are shown in Tables 1 and 2. The addition ratio of catalysts and water in the tables were calculated based on the total weight of a raw material compound of the formula (1), epichlorohydrin, catalyst and water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074946B2
Source datasetuspto-grants-2006_07
ORD IDord-4cfd76072bfd4a1c94c3b2d643eab6cf
Source noteuspto-grants-2006_07