反应 #171240
ord-d62525f5399940848ed10960d5b3ee0d
反应方程式
反应条件
后处理
- 1其他after completion of the reaction
- 2workup.STIRRINGthe mixture was stirred at room temperature overnight
- 3萃取extracted 6 times with diethyl ether (135 ml)
- 4其他The solvent of the obtained organic layer was evaporated under reduced pressure
- 5workup.ADDITIONDiethylether (450 ml) and water (150 ml) were added to the oil
- 6浓缩after concentration
- 7其他to allow partitioning
- 8萃取the aqueous layer was extracted 3 times with ethyl acetate (150 ml)
- 9干燥The combined organic layer was dried over anhydrous sodium sulfate
- 10其他the solvent was evaporated under reduced pressure
- 11浓缩The oil (10.1 g) after concentration
- 12其他was purified by chromatography (silica gel; 250 g, eluate; 50:1→3:1 hexane-ethyl acetate)
实验过程
3,7,11,15-Tetramethyl-hexadecan-1-ol (8.96 g, 30.0 mmol) was dissolved in a mixed solvent of acetone (360 ml) and acetic acid (180 ml), a solution of anhydrous chromic acid (7.27 g, 72.7 mmol) in water (9.0 ml) was added dropwise, and the mixture was stirred at room temperature for 1 hr. A solution of sodium disulfite (100 g, 526 mmol) in water (450 ml) was added to the reaction mixture after completion of the reaction, the mixture was stirred at room temperature overnight and extracted 6 times with diethyl ether (135 ml). The solvent of the obtained organic layer was evaporated under reduced pressure. Diethylether (450 ml) and water (150 ml) were added to the oil after concentration to allow partitioning, and the aqueous layer was extracted 3 times with ethyl acetate (150 ml). The combined organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The oil (10.1 g) after concentration was purified by chromatography (silica gel; 250 g, eluate; 50:1→3:1 hexane-ethyl acetate) to give the title compound (6.78 g, 72.3%) as a pale-blue oil.