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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473403생성일: 2026년 10월 25일

Ethylene Glycol → 2-(1,3-Dioxolan-2-yl)-3-nitropyridine

https://huagongshe.com/reaction/473403

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물WaterHCID 962—
반응물p-Toluenesulfonic acidHCID 6101—
반응물3-NitropicolinaldehydeHCID 329361—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(1,3-Dioxolan-2-yl)-3-nitropyridineHCID 329362—

반응 조건

온도120 °C

반응 단계

3-Nitro-2-pyridinecarbaldehyde (22 g, 144.74 mmol) was dissolved in toluene (500 mL). To the mixture was added catalytic amount of p-TSA (2 g) and ethylene glycol (40 mL) and the reaction flask equipped with Dean-Stark assembly was refluxed for 12 h at 120° C. After the reaction was complete, the reaction mixture was treated with water and ethyl acetate. The organic layer was separated and the aqueous layer was back extracted with ethyl acetate. The organic layers were combined and dried over anhydrous Na2SO4 and concentrated under reduced pressure to give a thick oily mass. The oily mass was then purified by silica gel column chromatography using 20% of ethyl acetate and hexane as eluent to give 2-(1,3-dioxolan-2-yl)-3-nitropyridine: 1H-NMR (CDCl3) δ: 4.2 (d, 5H), 6.5 (s, 1H), 7.5 (m, 1H), 8.3 (d, 1H), 8.9 (brs, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633313B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-0e6942b0b24047c6b74d017462bca360
출처 메모uspto-grants-2014_01