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Sulfuric Acid → 5-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamide

HRID 2406116
ノート
印刷プレビュー

反応式

HRID 2406116 の反応式
S(=O)(=O)(O)O.[NH2:6][C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:10]=[CH:9][C:8]=1[C:19]#[N:20].[OH-:21].[Na+]>>[NH2:6][C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:10]=[CH:9][C:8]=1[C:19]([NH2:20])=[O:21]
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 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 121505575-amino-1-(2-methylphenyl)-1H-pyrazole-4-carbonitrile

生成物 1

HCID 119839075-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamide

反応条件

温度
40 °C

実験手順

300 ml of 96% strength sulphuric acid are cautiously added to 40.0 g (201.8 mmol) of 5-amino-1-(2-methylphenyl)-1H-pyrazole-4-carbonitrile (Example 9A) while cooling in ice. The mixture is then heated to 40° C. and stirred for 2 hours at this temperature. After cooling, it is poured into 2 l of ice-water and cautiously neutralized with 50% strength sodium hydroxide solution. After extraction with ethyl acetate three times (2 l each time) the combined organic phases are washed with saturated sodium chloride solution and dried over sodium sulphate, and the solvent is distilled off under reduced pressure. 36.0 g (82% of theory) of product (purity >90%) are obtained and are employed without further purification in subsequent reactions.

後処理

  1. temperaturewhile cooling in ice
  2. temperatureAfter cooling
  3. extractionAfter extraction with ethyl acetate three times (2 l each time) the combined organic phases
  4. washare washed with saturated sodium chloride solution
  5. dry with materialdried over sodium sulphate
  6. distillationthe solvent is distilled off under reduced pressure
  7. custom36.0 g (82% of theory) of product (purity >90%) are obtained
  8. customare employed without further purification in subsequent reactions

出典と根拠

ORDレコード
ord-682f900a3a924b3dad276c37f70f2047
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08809348B2

反応ノート

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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