Реакция #1670
ord-3aaa2f0964b0473a962a140eaa35f34c
Уравнение реакции
ammonium chloride
NaH
pyridinone
hexane ethyl acetate
1-bromo-2-pentyne
→
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
Реагенты
Нет
Растворители
Условия реакции
Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1workup.WAITThe resulting mixture was kept at 0° C. during one half hour
- 2ЭкстракцияThe aqueous suspension was extracted with ether (3×100 ml)
- 3Промывкаthe combined ether layers washed with brine
- 4Другоеdried
- 5Другоеyielding the crude product
Методика
To a suspension of NaH (60% in mineral oil, 200 mg) in dry DMF (50 ml) at 0° C. was added the preceding pyridinone and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne dropwise. The resulting mixture was kept at 0° C. during one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml) and the combined ether layers washed with brine and dried, yielding the crude product. After column chromatography (silica gel, hexane:ethyl acetate 8:2) the product was obtained as a white amorphous solid.