تفاعل #171240
ord-d62525f5399940848ed10960d5b3ee0d
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىafter completion of the reaction
- 2workup.STIRRINGthe mixture was stirred at room temperature overnight
- 3استخلاصextracted 6 times with diethyl ether (135 ml)
- 4أخرىThe solvent of the obtained organic layer was evaporated under reduced pressure
- 5workup.ADDITIONDiethylether (450 ml) and water (150 ml) were added to the oil
- 6تركيزafter concentration
- 7أخرىto allow partitioning
- 8استخلاصthe aqueous layer was extracted 3 times with ethyl acetate (150 ml)
- 9تجفيفThe combined organic layer was dried over anhydrous sodium sulfate
- 10أخرىthe solvent was evaporated under reduced pressure
- 11تركيزThe oil (10.1 g) after concentration
- 12أخرىwas purified by chromatography (silica gel; 250 g, eluate; 50:1→3:1 hexane-ethyl acetate)
الإجراء التجريبي
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.