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
- 100 °C
PROCEDURE
实验过程
2-Hydroxy-4-methoxybenzaldehyde (5 g, 32.9 mmol), 1-bromodocosane (16.6 g, 42.7 mmol) and potassium carbonate (14.8 g, 107 mmol) were mixed with DMF (150 ml), and the mixture was stirred at 100° C. for 7 hr. Chloroform (400 ml) and 1N hydrochloric acid (300 ml) were added to the reaction mixture, and the mixture was washed. The organic layer was washed successively with 1N hydrochloric acid and saturated brine. The organic layer was concentrated and slurry-washed with methanol. The precipitate was collected by filtration and dried under reduced pressure. The obtained dried crystals were dissolved in THF (150 ml), sodium borohydride (3.7 g) was added, and the mixture was stirred at 40° C. for 3 hr. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was concentrated. The mixture was extracted with chloroform, and washed successively with aqueous sodium hydrogen carbonate solution and saturated brine. The organic layer was concentrated. The obtained residue was washed with acetonitrile, and the precipitate was collected by filtration and dried under reduced pressure to give 2-docosyloxy-4-methoxybenzyl alcohol (9.8 g).
WORKUP
后处理
- washthe mixture was washed
- washThe organic layer was washed successively with 1N hydrochloric acid and saturated brine
- concentrationThe organic layer was concentrated
- washslurry-washed with methanol
- filtrationThe precipitate was collected by filtration
- customdried under reduced pressure
- customThe obtained dried crystals
- dissolutionwere dissolved in THF (150 ml)
- additionsodium borohydride (3.7 g) was added
- stirringthe mixture was stirred at 40° C. for 3 hr
- addition1N Hydrochloric acid was added to the reaction mixture
- concentrationthe mixture was concentrated
- extractionThe mixture was extracted with chloroform
- washwashed successively with aqueous sodium hydrogen carbonate solution and saturated brine
- concentrationThe organic layer was concentrated
- washThe obtained residue was washed with acetonitrile
- filtrationthe precipitate was collected by filtration
- customdried under reduced pressure