反応式
[BH4-].[Na+].[CH3:3][C:4]1[CH:5]=[CH:6][C:7]([C:10](OC)=[O:11])=[N:8][CH:9]=1>C1COCC1.CO>[CH3:3][C:4]1[CH:5]=[CH:6][C:7]([CH2:10][OH:11])=[N:8][CH:9]=1参加物
5
実験手順
Sodium borohydride (4.5 g, 115. mmol) was added to a solution of methyl 5-methylpicolinate (6.0 g, 39.5 mmol) in THF (60 mL) and methanol (6 ml) at RT. The reaction mixture was stirred at RT for 2 h (the reaction was monitored by TLC). The mixture was concentrated under reduced pressure and the residue was diluted with water and extracted with EtOAc. The combined organics were dried over sodium sulfate, filtered and concentrated under reduced pressure. The organic layer was concentrated under vacuo to afford (5-methylpyridin-2-yl)methanol (3.5 g, 72.9%) as an off-white solid. 1H NMR: 200 MHz, CDCl3: δ 8.5 (s, 1H), 7.7 (d, 1H), 7.15 (d, 1H), 5.0 (s, 3H), 3.4 (s, 3H). MS: [M+H]+: m/z=124.0.
後処理
- concentrationThe mixture was concentrated under reduced pressure
- additionthe residue was diluted with water
- extractionextracted with EtOAc
- dry with materialThe combined organics were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- concentrationThe organic layer was concentrated under vacuo
出典と根拠
- ORDレコード
- ord-225c87e4b9234500abbf9627801447ba
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08343973B2
関連ノート
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