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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250942생성일: 2026년 10월 26일

Sodium Thiosulfate → 3-Allyloxy-pyridine-2-carbaldehyde

https://huagongshe.com/reaction/250942

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ThiosulfateHCID 24477—
반응물TriacetoxyperiodinaneHCID 159087—
반응물Sodium BicarbonateHCID 516892—
반응물(3-Allyloxy-pyridin-2-yl)-methanolHCID 14598977—
용매DichloromethaneHCID 6344—
생성물3-Allyloxy-pyridine-2-carbaldehydeHCID 4509099398.2%

반응 단계

To a solution of (3-allyloxy-pyridin-2-yl)-methanol (2.08 g, 12.6 mmol) (Chen, Y. L. Eur. Pat. Appl. (1985), EP 150984) in CH2Cl2 (60 mL) was added Dess-Martin Periodinane (5.82 g, 13.7 mmol), and stirred at room temperature for 24 hours. CH2Cl2 (40 mL), saturated NaHCO3 (30 mL), and aqueous sodium thiosulfate (30 mL) were added and stirred for 40 minutes. The layers were separated and the aqueous phase was extracted with CH2Cl2 (2×50 mL). The combined organic extracts were washed with brine (1×75 mL), dried (Na2SO4), and concentrated to provide 2.02 g (98%) of 3-allyloxy-pyridine-2-carbaldehyde as a brown oil. 1H NMR (CDCl3) δ 4.71 (d, 2H, J=6.0 Hz), 5.37 (d, 1H, J=12.0 Hz), 5.50 (d, 1H, J=18.0 Hz), 5.99-6.12 (m, 1H), 7.38-7.48 (m, 2H), 8.40 (d, 1H, J=3.0 Hz), 10.41 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-907f21e5df2c46b1ae1bf9c3040237c7
출처 메모uspto-grants-2011_01