Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Ethyl 4-bromo-3-oxobutanoate | HCID 575284 | — |
| Edukt | Thiobenzamide | HCID 683563 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 2-(2-phenyl-1,3-thiazol-4-yl)acetate | HCID 2797666 | — |
Reaktionsschritte
Ethyl γ-bromoacetoacetate [2.62 g, 0.9-1.0 mole, described by A. Burger and G. E. Ullyot, J. Org. Chem., 12, 346 (1947)]is added in one portion to a suspension of thiobenzamide [117.5 g, 0.857 mole, described by A. Silberg et al., Ber., 94, 2887 (1961)] in ethanol. The clear solution is refluxed on a steam bath for 2 hr, cooled and slowly added with stirring to ether (3500 ml). The white crystalline precipitate is collected, washed with ether and partitioned between water and ether. Sodium bicarbonate is added in portions until the mixture is alkaline. The mixture is extracted with ether, the ether solution is washed with saturated sodium chloride solution, dried, and evaporated to give ethyl 2-phenylthiazole-4-acetate (VII; R1 = H, R9 = CH2CH3), γmaxCHCl3 1725 cm-1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04033977 |
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| Quelldatensatz | uspto-grants-1977_07 |
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| ORD ID | ord-2964eaeb2c594e1793a3fd1e6a96a762 |
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| Quellennotiz | uspto-grants-1977_07 |
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