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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638056Generated: October 30, 2026

Epichlorohydrin → HCID 20255152, compound

https://huagongshe.com/reaction/638056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 136136665HCID 136136665—
ProductHCID 20255152HCID 20255152—

Reaction Steps

A mixture of 5 ml of epichlorohydrin and 0.5 g of potassium carbonate is heated under reflux. 0.5 g of 2-(4-hydroxyphenyl)-4-(trifluoromethyl)-thiazole is added in one portion and the reaction mixture is then heated under reflux for a further 15 minutes. After cooling, the mixture is filtered, the filtrate is concentrated by evaporation in a rotary evaporator and the residue is taken up in 6 ml of dichloromethane; 100 mg of tetrabutylammonium hydrogen sulphate and 6 ml of 2N sodium hydroxide solution are added to the solution and the whole is stirred for 3 hours at room temperature. The organic phase is separated off, washed and dried and finally the solvent is removed in a rotary evaporator. The residue is crystallised from ether/hexane yielding 2-[4-(2,3-epoxypropoxy)-phenyl]-4-(trifluoromethyl)-thiazole having a melting point of 97°-98°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559354
Source datasetuspto-grants-1985_12
ORD IDord-b1adad90d6354855807efd2571c8d79a
Source noteuspto-grants-1985_12