Water → Methyl 2-methoxyisonicotinate
反応式
Cl[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][N:10]=1)[C:5]([OH:7])=[O:6].[CH3:11][O-:12].[Na+].I[CH3:15].O>CN(C=O)C.CO>[CH3:11][O:12][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][N:10]=1)[C:5]([O:7][CH3:15])=[O:6]参加物
反応条件
- 温度
- 130 °C
実験手順
Under a nitrogen atmosphere, to a solution of 2-chloroisonicotinic acid (10.0 g) in DMF (150 mL) was added a 28% solution of sodium methoxide in methanol (38.6 mL), and the mixture was stirred at 130° C. for 14 hr. Iodomethane (15.9 mL) was added to the reaction mixture at 80° C., and the mixture was stirred at 80° C. for 5 min. Water was added at 0° C., and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine, and dried over anhydrous magnesium sulfate. After silica gel filtration, the solvent was evaporated under reduced pressure to give a crude product of the title compound (8.57 g) as a pale-yellow oil. This compound was used for the next step without further purification.
後処理
- stirringthe mixture was stirred at 80° C. for 5 min
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationAfter silica gel filtration
- customthe solvent was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-2b4fb410e6c64fd18569240a7f709725
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09181186B2
反応ノート
読み込み中…