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Phosphorus oxychloride → 5-Acetyl-3-pyridinecarbonitrile

HRID 1491839
ノート
印刷プレビュー

反応式

HRID 1491839 の反応式
P(Cl)(Cl)(Cl)=O.[C:6]([C:9]1[CH:10]=[N:11][CH:12]=[C:13]([C:15](=O)[NH2:16])[CH:14]=1)(=[O:8])[CH3:7]>CN(C)C=O>[C:6]([C:9]1[CH:10]=[N:11][CH:12]=[C:13]([C:15]#[N:16])[CH:14]=1)(=[O:8])[CH3:7]
参加物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 24813Phosphorus oxychlorideHCID 226073883-Pyridinecarboxamide, 5-acetyl-

生成物 1

HCID 189537855-Acetyl-3-pyridinecarbonitrile収率 48.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Phosphorus oxychloride (2.75 g) was added to a solution of 3-acetyl-5-carbamoylpyridine (2.8 g) in N,N-dimethylformamide (30 ml) with cooling on an ice-water bath. The mixture was stirred with cooling for 1.5 hours. The solvent was removed under reduced pressure. The residue was dissolved in water (150 ml) and the mixture was extracted with ethyl acetate (100 ml). The extract was dried with magnesium sulfate and then evaporated. The residue was chromatographed on a silica gel column eluting with chloroform to afford 3-acetyl-5-cyanopyridine (1.21 g).

後処理

  1. temperaturewith cooling on an ice-water bath
  2. temperaturewith cooling for 1.5 hours
  3. customThe solvent was removed under reduced pressure
  4. dissolutionThe residue was dissolved in water (150 ml)
  5. extractionthe mixture was extracted with ethyl acetate (100 ml)
  6. dry with materialThe extract was dried with magnesium sulfate
  7. customevaporated
  8. customThe residue was chromatographed on a silica gel column
  9. washeluting with chloroform

出典と根拠

ORDレコード
ord-825ce53b496c41359a5e94f82879672c
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05371097

反応ノート

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