Hydrochloric Acid → 1-phenyl-1H-pyrazol-5-ol
反応式
C(OC([C:6]1[C:10](=[O:11])[N:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[NH:8][CH:7]=1)=O)C.Cl>[OH-].[Na+]>[C:12]1([N:9]2[C:10](=[O:11])[CH:6]=[CH:7][NH:8]2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
4
実験手順
4-Ethoxycarbonyl-1-phenyl-3-pyrazolin-5-one (2.139 g, 9.2 mmol) in 1N sodium hydroxide (50 ml) was stirred under nitrogen at vigorous reflux for three hours. The reaction mixture was allowed to cool and acidified (HCl) to pH 3.5, whereupon ethyl acetate extraction, followed by drying (MgSO4) and evaporation produced the desired product (1.072 g, 72%) δ max(CHCl3) 1705, 1595, 1495 cm-1 δ(D6 -DMSO) 5.60 (1H,d,J2 Hz, C4 proton), 7.60 (6H, m, phenyl protons and C3 proton) Found; M+ ; 160.0641. C9H8N2O6 requires M; 160.0637.
後処理
- temperatureat vigorous reflux for three hours
- temperatureto cool
- extractionwhereupon ethyl acetate extraction
- customby drying
- custom(MgSO4) and evaporation
出典と根拠
- ORDレコード
- ord-e552ae1ab9a741ab8e60d2c0b06aecd9
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04537886
反応ノート
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