HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270141Erstellt: 25. Oktober 2026
Dimethylformamide → Ethyl 4-(hydroxymethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/270141
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 4-Bromomethyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic Acid Ethyl Ester | HCID 17951768 | — |
| Katalysator | Silver trifluoroacetate | HCID 76299 | — |
| Produkt | Ethyl 4-(hydroxymethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylate | HCID 17951856 | — |
Reaktionsschritte
To a stirred solution of ethyl 4-(bromomethyl)-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylate (50g, 0.127moles, 1eq) in dry DMF (300ml) under a positive N2flow was added silver trifluoroacetate (42.02g, 0.191moles, 1.5eq) all at once as a solid. This was stirred at room temperature for 3.5hrs. The reaction was partitioned between ethyl ether (1.5L) and water (500ml). The phases were separated and the organic phase washed twice with water (500ml). After separation of the phases, the organic fraction was dried with Na2SO4, filtered and concentrated in vacuo. The crude trifluoroacetate product was used without characterization. Ethanol (300ml) was added and the reaction was refluxed for 10hrs. After cooling to room temperature the ethanol was removed in vacuo to yield 42g (100%) of the title compound. The product was used without purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07449468B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-84103e99eb8f405e9db2c76f2e4b7ca6 |
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| Quellennotiz | uspto-grants-2008_11 |
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