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1,4-Dioxane → 5-Nitropyridine-2-carbaldehyde

HRID 55875
ノート
印刷プレビュー

反応式

HRID 55875 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.[O:11]1CCOCC1>>[N+:8]([C:5]1[CH:6]=[CH:7][C:2]([CH:1]=[O:11])=[N:3][CH:4]=1)([O-:10])=[O:9]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 312751,4-DioxaneHCID 27945522-Methyl-5-nitropyridine

生成物 1

HCID 151455015-Nitropyridine-2-carbaldehyde収率 58%

反応条件

温度
80 °C

実験手順

To a stirred solution of compound 2-methyl-5-nitropyridine (30) (10 g, 72.5 mmol) in 1,4-dioxane (150 mL) was added SeO2 (9.5 g, 87.0 mmol) at room temperature. The resulting reaction mixture was stirred at 80° C. for 16 h. The reaction mixture was evaporated, the residue was diluted with water (100 mL), the resulting precipitate was separated by filtration and the filtrate was extracted with ethyl acetate (3×100 mL). The combined organic layer was washed with water (100 mL), brine (100 mL), the organic layer was dried over Na2SO4 and concentrated to give 31 (6.4 g, 58%) as a brown solid. Rf: 0.7 (30% EtOAc/pet-ether); 1H NMR (400 MHz, CDCl3): δ 10.18 (1H, s), 9.59 (1H, d, J=2.0 Hz), 8.68-8.65 (1H, m), 8.16 (1H, d, J=8.4 Hz)

後処理

  1. customThe resulting reaction mixture
  2. customThe reaction mixture was evaporated
  3. additionthe residue was diluted with water (100 mL)
  4. customthe resulting precipitate was separated by filtration
  5. extractionthe filtrate was extracted with ethyl acetate (3×100 mL)
  6. washThe combined organic layer was washed with water (100 mL), brine (100 mL)
  7. dry with materialthe organic layer was dried over Na2SO4
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7e534fcb9fae4cd794b52f9c55d79f1e
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09433622B2

反応ノート

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