反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
(Methoxymethyl)triphenylphosphonium chloride (26.73 g, 78 mmole) was suspended in absolute THF (90 ml) under argon, potassium tert-butylate (8.75 g, 78 mmole), dissolved in absolute THF (90 ml), was added dropwise at 0° C., and the mixture was then stirred for 15 minutes at 0° C. The aldehyde 9b (13.69 g, 52 mmole), dissolved in absolute THF (90 ml), was then added dropwise at RT and the mixture was stirred overnight at RT. The mixture was hydrolysed by dropwise addition of water (50 ml) and 6N HCl (150 ml), while cooling with iced water. After stirring for one hour at RT the mixture was extracted 10 times with ether (each time 50 ml). The aqueous phase was adjusted to pH 11 with 5N NaOH, shaken three times with ethyl acetate (each time 100 ml), dried over Na2 SO4 and concentrated by evaporation in vacuo. The crude product was purified by flash chromatography with ethyl acetate/cyclohexane (1:1).
WORKUP
后处理
- additionwas added dropwise at 0° C.
- additionwas then added dropwise at RT
- stirringthe mixture was stirred overnight at RT
- stirringAfter stirring for one hour at RT the mixture
- extractionwas extracted 10 times with ether (each time 50 ml)
- stirringshaken three times with ethyl acetate (each time 100 ml),
- customdried over Na2 SO4
- concentrationconcentrated by evaporation in vacuo
- customThe crude product was purified by flash chromatography with ethyl acetate/cyclohexane (1:1)