Hydrochloric Acid → 4-Nitro-1-phenyl-1H-pyrazole-3-carboxylic acid
反応式
C([O:3][C:4]([C:6]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][N:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:7]=1)=[O:5])C.[OH-].[Na+].Cl.O>C(O)C>[N+:11]([C:10]1[C:6]([C:4]([OH:5])=[O:3])=[N:7][N:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:9]=1)([O-:13])=[O:12]参加物
6
実験手順
To a stirred suspension of 4-nitro-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester (240 mg, 0.92 mmol) at rt in ethanol (3 ml) under an argon atmosphere was added 1 N NaOH (1.8 ml). The mixture was stirred for 2 hrs. 3 N HCl was added until pH˜2 was reached. Upon addition of H2O (˜2 ml), the product precipitated out. It was collected by filtration, washed with H2O and dried. Off-white solid (184 mg, 86%).
後処理
- customthe product precipitated out
- filtrationIt was collected by filtration
- washwashed with H2O
- customdried
出典と根拠
- ORDレコード
- ord-fe57542f218042a18d92b988f02729b1
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08703768B2
反応ノート
読み込み中…