Реакция #2358524
ord-0e4f4e4a4e7f4d82a5a8aa1541f20587
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1Температураcooled to room temperature
- 2ЭкстракцияThe aqueous phase was extracted with ethyl acetate (2×100 ml)
- 3ПромывкаThe combined organic phase was washed with aqueous NaOH (3 M, 50 ml) and brine (75 ml)
- 4Сушкаdried (Na2SO4)
- 5Другоеevaporated
- 6ДругоеPurification by flash column chromatography (ethyl acetate/isooctane, 0:1 to 1:0)
Методика
A mixture of triphenylphosphine (1.9 g, 7.3 mmol) in dry THF (20 ml) was flushed with N2(g) and DEAD (3.1 ml, 6.9 mmol) was added drop-wise, 1.2-dibromoethane followed by 3-fluoro-5-methylsulfonyl-phenol (1.1 g, 6.1 mmol) and then boc-glycinol (1.0 ml, 6.1 mmol) in portions. The mixture was stirred at 70° C. for 20 h, cooled to room temperature and water and EtOAc was added. The aqueous phase was extracted with ethyl acetate (2×100 ml). The combined organic phase was washed with aqueous NaOH (3 M, 50 ml) and brine (75 ml), dried (Na2SO4) and evaporated. Purification by flash column chromatography (ethyl acetate/isooctane, 0:1 to 1:0) gave the title compound (1.4 g, 70%). MS m/z (relative intensity, 70 eV 298 (M+, 18), 296 (M+, 18), 109 (bp), 107 (99), 82 (15).