Réaction #1605
ord-d9ff793142c547c8aee4d9d896a93b93
Équation de réaction
ammonium chloride
quinolinone
NaH
1-bromo-2-pentyne
→
product
5-chloro-1-(2-pentyn-1-yl)-2-quinolinone
Réactifs
Aucun
Conditions de réaction
Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.WAITThe resulting mixture was kept at 0° C. for one half hour
- 2ExtractionThe aqueous suspension was extracted with ether (3×100 ml)
- 3Lavagethe combined ether layers washed with brine
- 4Autredried
- 5Autreyielding the crude product
Mode opératoire
To a suspension of NaH (60% in mineral oil, 700 mg) in dry DMF (100 ml) at 0° C. was added the preceding quinolinone (2.05 g) and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne (1.6 g) dropwise. The resulting mixture was kept at 0° C. for one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml), the combined ether layers washed with brine and dried, yielding the crude product. Trituration with hexane yielded the product as a yellow solid (1 g).