Реакция #1857551
ord-0f38169136074e08a236cff97b848483
Уравнение реакции
Растворители
Условия реакции
Обработка
- 1Другоеat 0° C
- 2ДругоеThe flask was removed from the cold bath
- 3Температураcooled
- 4workup.ADDITIONmixture of diethyl ether (Et2O; 60 mL) and 2 Normal (N) HCl (20 mL) over 15 min
- 5ДругоеThe mixture was removed from the cold bath
- 6workup.STIRRINGstirred at room temperature for 30 min
- 7ДругоеThe phases were separated
- 8Экстракцияthe aq. phase was further extracted with Et2O (2×50 mL)
- 9Промывкаwashed with sat. aq. sodium bicarbonate (NaHCO3; 25 mL) and brine (25 mL)
- 10Сушкаdried over Na2SO4
- 11Фильтрацияfiltered
- 12workup.ADDITIONthe filtrate treated with Celite® (5 scoopula tip-fulls)
- 13ДругоеThe solvent was removed under reduced pressure
- 14Другоеpurified
Методика
To a solution of (S)-methyl 2-((S)-1-((4-methoxybenzyl)oxy)ethyl)-5-methylhexanoate (6.00 g, 19.5 mmol) and chlorobis(cyclooctene)-iridium(I) dimer (0.349 g, 0.389 mmol) in dry DCM (19.5 mL) was slowly added Et2SiH (3.76 mL, 29.2 mmol) at 0° C. The flask was removed from the cold bath and the reaction was stirred at room temperature for 20 h under nitrogen (N2). The reaction mixture was transferred via cannula to an ice-cooled mixture of diethyl ether (Et2O; 60 mL) and 2 Normal (N) HCl (20 mL) over 15 min. The mixture was removed from the cold bath and stirred at room temperature for 30 min. The phases were separated and the aq. phase was further extracted with Et2O (2×50 mL). The organics were combined, washed with sat. aq. sodium bicarbonate (NaHCO3; 25 mL) and brine (25 mL), dried over Na2SO4, filtered, and the filtrate treated with Celite® (5 scoopula tip-fulls). The solvent was removed under reduced pressure and the resulting adsorbed material was directly loaded onto a column and purified using flash column chromatography (120 g SiO2, 0→75% EtOAc/hexanes) to afford the intermediate aldehyde, (S)-2-((S)-1-((4-methoxybenzyl)oxy)ethyl)-5-methylhexanal.