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HRID 17927作成日:2026年10月27日

p-Toluenesulfonic acid → 2-(2,2-Dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrile

https://huagongshe.com/reaction/17927

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物2,2-DimethoxypropaneHCID 6495—
反応物2-(3,4-Dihydroxyphenyl)acetonitrileHCID 10909727—
溶媒TolueneHCID 1140—
生成物2-(2,2-Dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrileHCID 5526773220%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741321B2
出典データセットuspto-grants-2010_06
ORD IDord-7a337b278ba646a3833ed2f50bf91956
出典メモuspto-grants-2010_06