참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Thiosulfate | HCID 24477 | — |
| 반응물 | Triacetoxyperiodinane | HCID 159087 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (3-Allyloxy-pyridin-2-yl)-methanol | HCID 14598977 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-Allyloxy-pyridine-2-carbaldehyde | HCID 45090993 | 98.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863293B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-907f21e5df2c46b1ae1bf9c3040237c7 |
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| 출처 메모 | uspto-grants-2011_01 |
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