3-Amino-1-phenylpyrazole → 1-phenyl-1H-pyrazol-3-amine

HRID 26274

反応式

HRID 26274 の反応式
[C:1]1([N:7]2[CH2:11][CH2:10][C:9]([NH2:12])=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(=O)(O)[O-].[Na+]>C(O)(=O)C.Cl[Cu]>[C:1]1([N:7]2[CH:11]=[CH:10][C:9]([NH2:12])=[N:8]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参加物

5

反応物 2

HCID 987363-Amino-1-phenylpyrazoleHCID 516892Sodium Bicarbonate

生成物 1

HCID 5943201-phenyl-1H-pyrazol-3-amine収率 30.4%

試薬・触媒・溶媒 2

HCID 62652Cuprous chloride触媒HCID 176Acetic Acid溶媒2 回

実験手順

Using the same apparatus as in Example 1 and following the same modalites, 5 g (0.031 mole) of 1-phenyl-3-amino-2-pyrazoline were dissolved in 15 ml of acetic acid with addition of 0.2 g (0.00201 mole) of CuCl, under an oxygen head. Oxidation was completed after about 5 hours. Acetic acid was neutralized with sodium bicarbonate, it was filtered and the precipitate was extracted with ether. By evaporating the ethereal solution, 1.5 g of 1-phenyl-3-aminopyrazole were obtained.

後処理

  1. filtrationwas filtered
  2. extractionthe precipitate was extracted with ether
  3. customBy evaporating the ethereal solution

出典と根拠

ORDレコード
ord-7d675656b0164059bb07db0ee5f118df
出典データセット
uspto-grants-1979_04
特許番号
US04149005

関連ノート

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