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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473404생성일: 2026년 10월 25일

2-(1,3-Dioxolan-2-yl)-3-nitropyridine → 2-(1,3-Dioxolanyl)-3-aminopyridine

https://huagongshe.com/reaction/473404

반응식

참여 물질

역할이름HCID투입량
반응물2-(1,3-Dioxolan-2-yl)-3-nitropyridineHCID 329362—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-(1,3-Dioxolanyl)-3-aminopyridineHCID 329363—

반응 단계

2-(1,3-Dioxolan-2-yl)-3-nitropyridine (10 g, 51 mmol) was suspended in ethanol (300 mL). To the mixture was added 10% Pd/C (3 g). The reaction mixture was kept at 60 psi pressure using Parr-shaker hydrogenation assembly. After completion of reaction (6 h), the reaction mixture was filtered through Celite™ and the filtrate was concentrated under reduced pressure to give 2-(1,3-dioxolan-2-yl)-3-pyridinamine as an off orange solid: 1H-NMR (CDCl3) δ: 4.4-4.0 (m, 6H), 5.8 (s, 1H), 7.2-6.9 (m, 2H), 8.0 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633313B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-778566ff162e40edae60b03cebeebc31
출처 메모uspto-grants-2014_01