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6-Bromo-3-pyridinecarboxaldehyde → 5-Formylpyridine-2-carbonitrile

HRID 627624
ノート
印刷プレビュー

反応式

HRID 627624 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[O:9])=[CH:4][N:3]=1.[Cu][C:11]#[N:12]>CN(C=O)C>[CH:8]([C:5]1[CH:6]=[CH:7][C:2]([C:11]#[N:12])=[N:3][CH:4]=1)=[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

4

反応物 2

HCID 117692346-Bromo-3-pyridinecarboxaldehydeHCID 178418546HCID 178418546、化合物

生成物 1

HCID 109862635-Formylpyridine-2-carbonitrile収率 35.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
120 °C

実験手順

A suspension of 2-bromo-5-formylpyridine (940 mg, 5.05 mmol) and copper (I) cyanide (679 mg, 7.58 mmol) in DMF (8.4 mL) was stirred at 120° C. for 1.5 hours, cooled to RT, and partitioned between water and EtOAc. The solids were removed from the aqueous layer by filtration, and the filtrate was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The crude product was purified by silica-gel chromatography, eluting with a gradient of 40%-60% (40% ethyl acetate in heptane) in heptane, to provide the title compound (236 mg, 1.786 mmol) as white solid. LC/MS (ESI+) m/z=133 (M+H).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturecooled to RT
  2. custompartitioned between water and EtOAc
  3. customThe solids were removed from the aqueous layer by filtration
  4. extractionthe filtrate was extracted with ethyl acetate
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe crude product was purified by silica-gel chromatography
  10. washeluting with a gradient of 40%-60% (40% ethyl acetate in heptane) in heptane

出典と根拠

ORDレコード
ord-518ed2a9eced4e31b33011be97fb09cf
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309263B2

反応ノート

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