HRID1195860
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
5-Hydroxy-2-(4-methyl-3-pentenyl)-5-(2-trimethylsilyl-4-furyl)-2-pentenal (0.88 g, 0.274 mmol) was dissolved in 27 ml anhydrous benzene, placed in a quartz tube and deoxygenated by saturating with oxygen-free nitrogen for one hour. The solution was irradiated at 254 nm for three hours, cooled and concentrated to give a brown-yellow gum. This material was purified by flash chromatography (silica, 15 to 30% ethyl acetate/hexane). First eluted was the desired acetal followed by starting aldehyde.
WORKUP
后处理
- customplaced in a quartz tube
- customdeoxygenated
- concentrationby saturating with oxygen-free nitrogen for one hour
- customThe solution was irradiated at 254 nm for three hours
- temperaturecooled
- concentrationconcentrated
- customto give a brown-yellow gum
- customThis material was purified by flash chromatography (silica, 15 to 30% ethyl acetate/hexane)
- washFirst eluted