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
PROCEDURE
实验过程
(2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol (1.3 g, 6.0 mmol) was dissolved in cyclohexane (4.5 mL), added with aluminum isopropoxide (123 mg, 0.1 eq, 0.6 mmol) and 2-fluorobenzaldehyde (968 mg, 1.3 eq, 7.8 mmol) and stirred at room temperature for 3 hours. The reaction mixture was added with hexane, then made acidic with addition of 1 N hydrochloric acid and extracted twice with ethyl acetate. Subsequently, the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to obtain 1.23 g (yield: 92%, E:Z=99:1) of the title compound as yellow oil.
WORKUP
后处理
- extractionextracted twice with ethyl acetate
- washSubsequently, the organic layer was washed with saturated brine
- dry with materialdried over magnesium sulfate
- customThe solvent was evaporated in vacuo
- customthe residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1)