Reaktion #94198

Reaktionsgleichung

ethyl bromopyruvate

4-methylquinazoline

ethyl bromopyruvate

→

product

2-Carbethoxypyrrolo[1,2-c]quinazoline

Lösungsmittel

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturat reflux for two hours
2. 2
   SonstigeDuring this time, a tan solid formed
3. 3
   Temperaturto reflux overnight
4. 4
   SonstigeThe alcohol was removed in vacuo
5. 5
   workup.ADDITIONthe residue diluted with H2O
6. 6
   workup.ADDITIONSodium bicarbonate was added until effervescence
7. 7
   Extraktionthe aqueous mixture extracted with ether
8. 8
   Trocknendried over Na2SO4
9. 9
   Filtrationfiltered
10. 10
    Sonstigethe solvent removed in vacuo
11. 11
    Sonstigeto yield a tan solid
12. 12
    SonstigeCrystallization from MeOH

Vorschrift

A solution of ethyl bromopyruvate (3.2g, 0.016 m) and 4-methylquinazoline (2.0g, 0.014 m) in dry ethanol (150 ml) was heated at reflux for two hours. During this time, a tan solid formed. Excess ethyl bromopyruvate was added (1.0g) and the reaction mixture was allowed to reflux overnight. After this time, the reaction was complete. The alcohol was removed in vacuo and the residue diluted with H2O. Sodium bicarbonate was added until effervescence ceased and the aqueous mixture extracted with ether. The ether extracts were combined, dried over Na2SO4, filtered and the solvent removed in vacuo to yield a tan solid. Crystallization from MeOH afforded the product as a white solid; m.p. 138°-139° C.

Quelle