反应详情

1-Acetyl-3-(2-bromoethyl)-4,6-dimethylindoline (5.4 g), NaCN (3.7 g) and 18-crown-6 (480 mg) were suspended in CH3CN (50 ml), and the suspension was refluxed for 15 hr. CH3CN was evaporated under reduced pressure. CHCl3 (100 ml) was added, and the mixture was washed with water and dried over anhydrous sodium sulfate. CHCl3 was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: CHCl3/MeOH=50/1−10/1) to give 4.5 g of 1-acetyl-3-(2-cyanoethyl)-4,6-dimethylindoline.

1. temperaturethe suspension was refluxed for 15 hr
2. customCH3CN was evaporated under reduced pressure
3. additionCHCl3 (100 ml) was added
4. washthe mixture was washed with water
5. dry with materialdried over anhydrous sodium sulfate
6. customCHCl3 was evaporated under reduced pressure
7. customThe residue was purified by silica gel column chromatography (eluent: CHCl3/MeOH=50/1−10/1)