反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N+:6]([O-])=[C:5]([CH3:10])[CH:4]=1>CC(O)=O.[Fe]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([CH3:10])[CH:4]=1参加物
4
反応条件
- 温度
- 120 °C
実験手順
To a stirred solution of 4-methoxy-2-methylpyridine 1-oxide (20 g, 0.143 mol) in AcOH (200 mL, sdfine, India), was added Fe (16 g, 0.287 mol, sdfine, India) and the reaction mixture was stirred for 2 h at 120° C. The reaction mixture was concentrated and neutralized with sat'd NaHCO3. EtOAc was added to the mixture and it was filtered through Celite® brand filter agent. The organic layer was separated and the aqueous layer was extracted with EtOAc (3×150 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated to give the title compound as a brown liquid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.33 (d, J=6 Hz, 1H), 6.68-6.64 (m, 2H), 3.84 (s, 3H), 2.52 (s, 3H). MS (ESI, positive ion) m/z: 124.0 (M+H).
後処理
- concentrationThe reaction mixture was concentrated
- additionEtOAc was added to the mixture and it
- filtrationwas filtered through Celite® brand
- filtrationfilter agent
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with EtOAc (3×150 mL)
- dry with materialThe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-1fc9b8c7e57e4e74bcef376ed1d778ed
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09096527B2
関連ノート
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