HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1054225Erstellt: 25. Oktober 2026
Ethyl bromopyruvate → Ethyl 2-(trifluoromethyl)-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/1054225
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl bromopyruvate | HCID 66144 | — |
| Edukt | N-Ethyl(trifluoro)ethanethioamide | HCID 15499429 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 2-(trifluoromethyl)-1,3-thiazole-4-carboxylate | HCID 20079591 | 42% |
Reaktionsschritte
To a stirring solution of ethyl 2,2,2-trifluoroethanethioamide (0.35 g, 2.71 mmol) in THF (12 ml) was added ethyl bromo pyruvate (0.375 ml, 2.98 mmol) at RT. Reaction mixture was heated at 90-100° C. for 16 h. Reaction mixture was diluted with water and DCM. The organic layer was separated and distilled out to get crude product which was column purified using 0-2% EtOAC in hexane to get titled compound in 42% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09394300B2 |
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| Quelldatensatz | uspto-grants-2016_07 |
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| ORD ID | ord-448485750cbc4c689cacf333ad9151b2 |
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| Quellennotiz | uspto-grants-2016_07 |
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