Ammonium Chloride → 6-Chloro-3-pyridinecarbonitrile

HRID 1488724

反応式

HRID 1488724 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](Cl)(Cl)Cl)=[CH:4][N:3]=1.[Cl-].[NH4+:13]>C1(C)C(C)=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[N:13])=[CH:4][N:3]=1

参加物

4

実験手順

In a 200-ml reaction flask equipped with a thermometer, a Dimroth condenser and a stirrer were fed 46 g (0.2 mole) of 2-chloro-5-trichloromehtylpyridine, 16 g (0.3 mole) of ammonium chloride and 0.23 g (0.5% by weight) of cupric oxide. The mixture was reacted at 200° C. for 12 hours. The reaction mixture was cooled. At 130° C., 100 ml of xylene was added into the reaction flask. The mixture was cooled further. At 60° C., the mixture was filtered to remove a copper salt and excessive ammonium chloride. The filtrate (xylene layer) was concentrated. The resulting concentrate was subjected to distillation to obtain 20.3 g of 2-chloro-5-cyanopyridine as a fraction having a boiling point of 146°-150° C./15 mmHg. [Yield: 73.3%, colorless crystals having a melting point of 117°-118° C. (crystallization took place after distillation)]

後処理

  1. customIn a 200-ml reaction flask
  2. customequipped with a thermometer
  3. customThe mixture was reacted at 200° C. for 12 hours
  4. temperatureThe reaction mixture was cooled
  5. temperatureThe mixture was cooled further
  6. filtrationAt 60° C., the mixture was filtered
  7. customto remove a copper salt and excessive ammonium chloride
  8. concentrationThe filtrate (xylene layer) was concentrated
  9. concentrationThe resulting concentrate
  10. distillationwas subjected to distillation

出典と根拠

ORDレコード
ord-d1521787264849a985c23acfb0663c47
出典データセット
uspto-grants-1997_10
特許番号
US05675012

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