Sodium Hydroxide → 1-Phenyl-1H-pyrazole-5-carboxylic acid

HRID 329336ノート

反応式

HRID 329336 の反応式
[C:1]1([N:7]2[C:11]([C:12]([O:14]CC)=[O:13])=[CH:10][CH:9]=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>C(O)C>[C:1]1([N:7]2[C:11]([C:12]([OH:14])=[O:13])=[CH:10][CH:9]=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

4

実験手順

4.4 g of ethyl 1-phenylpyrazole-5-carboxylate from Example 1 were stirred for 6 hours at room temperature with 10 ml of 16.5% strength aqueous NaOH and 10 ml of ethanol; the ethanol was removed by distillation, the aqueous phase was extracted twice with 10 ml of toluene, and the pH was adjusted to 3 using concentrated HCl. The precipitate was filtered off under suction, washed with a little water and dried: 3.1 g of product of boiling point 182°-183° C. were obtained.

後処理

  1. customthe ethanol was removed by distillation
  2. extractionthe aqueous phase was extracted twice with 10 ml of toluene
  3. filtrationThe precipitate was filtered off under suction
  4. washwashed with a little water
  5. customdried

出典と根拠

ORDレコード
ord-59c2faa4046f49848394ef5f88208e15
出典データセット
uspto-grants-1990_01
特許番号
US04891057

反応ノート

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