反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][N:2]=1.[C:7]1([CH2:13]C(O)=O)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+]>OS(O)(=O)=O.[N+]([O-])([O-])=O.[Ag+]>[CH2:13]([C:5]1[CH:4]=[CH:3][N:2]=[N:1][CH:6]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1参加物
反応条件
- 温度
- 70 °C
実験手順
To a 70° C. solution of pyridazine (9; 10 g, 0.125 mole) in aqueous H2SO4 (2N, 125 mL) was added AgNO3 (6.37 g, 0.0375 mole). Phenylacetic acid (10; 85.06 g 0.625 mole) was added to the mixture. The reaction mixture was stirred vigorously at 70° C. for 20 minutes and was degassed with a flow of nitrogen for 2 minutes, followed by a slow portionwise addition of ammonium persulfate (85.62, 0.375 mole) with rapid gas evolution. The reaction mixture was then heated at 90° C. for 30 minutes. The reaction mixture was then cooled at room temperature and the solution was extracted with CH2Cl2. A 50% NaOH solution was added to the aqueous phase, which was re-extracted with CH2Cl2 twice. The combined extracts were dried over MgSO4. The solvent was evaporated to dryness and the residue was purified by silica gel chromatography using CH2Cl2/5% methanol as the eluent. The yield of 4-benzylpyridazine (11) obtained was 8.2 g or 39%. MS (ESI+): [M+H]+=171.47; 1H NMR (300 MHz, CDCl3), δ ppm: 4.0 (s, 2H), 7.18-7.4 (m, 6H), 9.02-9.18 (m, 2H).
後処理
- customwas degassed with a flow of nitrogen for 2 minutes
- temperatureThe reaction mixture was then heated at 90° C. for 30 minutes
- temperatureThe reaction mixture was then cooled at room temperature
- extractionthe solution was extracted with CH2Cl2
- additionA 50% NaOH solution was added to the aqueous phase, which
- extractionwas re-extracted with CH2Cl2 twice
- dry with materialThe combined extracts were dried over MgSO4
- customThe solvent was evaporated to dryness
- customthe residue was purified by silica gel chromatography
出典と根拠
- ORDレコード
- ord-62abfacfb8b24310b2b6190bcfb35355
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08895556B2
関連ノート
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