反应详情

To a solution of (3,4-dihydroxy-phenyl)-acetonitrile (0.2 g, 1.3 mmol) in toluene (4 mL) was added 2,2-dimethoxy-propane (0.28 g, 2.6 mmol) and TsOH (0.010 g, 0.065 mmol). The mixture was heated at reflux overnight. The reaction mixture was evaporated to remove the solvent and the residue was dissolved in ethyl acetate. The organic layer was washed with NaHCO3 solution, H2O, brine, and dried over Na2SO4. The solvent was evaporated under reduced pressure to give a residue, which was purified by column chromatography on silica gel (Petroleum Ether/EtOAc 10:1) to give 2-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrile (40 mg, 20%). 1H NMR (CDCl3, 400 MHz) δ 6.68-6.71 (m, 3H), 3.64 (s, 2H), 1.67 (s, 6H).

1. temperatureThe mixture was heated
2. temperatureat reflux overnight
3. customThe reaction mixture was evaporated
4. customto remove the solvent
5. dissolutionthe residue was dissolved in ethyl acetate
6. washThe organic layer was washed with NaHCO3 solution, H2O, brine
7. dry with materialdried over Na2SO4
8. customThe solvent was evaporated under reduced pressure
9. customto give a residue, which
10. customwas purified by column chromatography on silica gel (Petroleum Ether/EtOAc 10:1)