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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468233생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/468233

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2,2-DimethoxypropaneHCID 6495—
반응물2-(3,4-Dihydroxyphenyl)acetonitrileHCID 10909727—
용매TolueneHCID 1140—
생성물2-(2,2-Dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrileHCID 5526773220%

반응 단계

To a solution of (3,4-dihydroxy-phenyl)-acetonitrile (0.20 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/ethyl acetate 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623905B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-a12bac07e87b47d29c8dc7f96afe787a
출처 메모uspto-grants-2014_01