HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638056Generated: October 30, 2026
Epichlorohydrin → HCID 20255152, compound
https://huagongshe.com/reaction/638056
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 136136665 | HCID 136136665 | — |
| Product | HCID 20255152 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04559354 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-b1adad90d6354855807efd2571c8d79a |
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| Source note | uspto-grants-1985_12 |
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