Diethyl Carbonate → Ethyl 4-bromothiazole-2-carboxylate
Reaktionsgleichung
[Br:1][C:2]1[N:3]=[C:4](Br)[S:5][CH:6]=1.C([Mg]Cl)(C)C.[C:13](=O)([O:17]CC)[O:14][CH2:15][CH3:16]>C1COCC1>[CH2:15]([O:14][C:13]([C:4]1[S:5][CH:6]=[C:2]([Br:1])[N:3]=1)=[O:17])[CH3:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a solution of dibromothiazole (1 g, 4.15 mmol) in THF (15 mL) at 0° C., is added dropwise a solution of iPrMgCl in THF (2 M, 2.3 mL, 4.57 mmol, 1.10 equiv.). The reaction is stirred at 0° C. for 0.25 h. To the resulting orange solution is added via a cannula, diethyl carbonate (3 mL) in THF (5 ml). The resulting green solution is stirred further at room temperature for 0.5 h, at which point the reaction is quenched by adding saturated NH4Cl. The title compound is purified by LC using 6/4 cyclohexane/DCM as the eluent to afford 514.2 mg (52%) of the title compound as a pale yellow powdery solid.
Aufarbeitung
- stirringThe resulting green solution is stirred further at room temperature for 0.5 h, at which
- customis quenched
- additionby adding saturated NH4Cl
- customThe title compound is purified by LC
Quellen und Nachweise
- ORD-Eintrag
- ord-1842841737b94662a73ef1c8b5129fd1
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07915256B2
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