Ethyl benzoylacetate → 2-(3,5-Dichloro-phenyl)-5-phenyl-2,4-dihydro-pyrazol-3-one
反応式
[C:1]([CH2:9][C:10]([O:12]CC)=O)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[Cl:16][C:17]1[CH:18]=[C:19]([NH:24][NH2:25])[CH:20]=[C:21]([Cl:23])[CH:22]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C(O)C>[Cl:16][C:17]1[CH:18]=[C:19]([N:24]2[C:10](=[O:12])[CH2:9][C:1]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[N:25]2)[CH:20]=[C:21]([Cl:23])[CH:22]=1参加物
実験手順
A solution of ethyl benzoylacetate (0.192 g, 1.00 mmol), 3,5-dichlorophenylhydrazine hydrochloride (0.235 g, 1.10 mmol), and p-toluenesulfonic acid monohydrate (0.019 g, 0.10 mmol) in ethanol (10 mL) was heated at reflux for 24 hours. The reaction solution was concentrated and the resulting residue was partitioned between ethyl acetate and aqueous 1N hydrochloric acid solution. The organic layer was further washed with water and brine, dried (sodium sulfate) and concentrated to afford a yellow solid. The crude product was triturated with hexanes and collected by suction filtration. Air drying afforded 0.174 g (57%) of product as a bright yellow solid: 1H NMR (DMSO-d6) δ12.60-12.40 (br s, 1H), 7.92 (s, 2H), 7.87-7.83 (d, 2H), 7.50 (s, 1H), 7.44-7.38 (m, 2H), 7.36-7.31 (m, 1H), 6.02 (s, 1H) ppm.
後処理
- temperatureat reflux for 24 hours
- concentrationThe reaction solution was concentrated
- customthe resulting residue was partitioned between ethyl acetate and aqueous 1N hydrochloric acid solution
- washThe organic layer was further washed with water and brine
- dry with materialdried (sodium sulfate)
- concentrationconcentrated
- customto afford a yellow solid
- customThe crude product was triturated with hexanes
- filtrationcollected by suction filtration
- customAir drying
出典と根拠
- ORDレコード
- ord-291e57aaa3304f20bada8d4c01da3006
- 出典データセット
- uspto-grants-2002_06
- 特許番号
- US06410533B1
反応ノート
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