Formaldehyde → Methyl 1-methylpyrrolidine-2-carboxylate
反応式
[NH:1]1[CH2:5][CH2:4][CH2:3][CH:2]1[C:6]([O:8][CH3:9])=[O:7].C=O.[C:12]([BH3-])#N.[Na+]>CO>[CH3:12][N:1]1[CH2:5][CH2:4][CH2:3][CH:2]1[C:6]([O:8][CH3:9])=[O:7]参加物
反応条件
- 温度
- 2.5 °C
実験手順
Methyl pyrrolidine-2-carboxylate 10b crude product (5 g) was dissolved in 100 mL of methanol. The solution was cooled to 0-5° C. in an ice-water bath, followed by addition of 13 mL of 40% formaldehyde. The reaction mixture was warmed up to room temperature and stirred for 2 hours, then cooled to 0-5° C. in an ice-water bath, and sodium cyanoborohydride (5.45 g, 87.20 mmol) was added in batches. The reaction mixture was warmed up to room temperature and stirred for 24 hours. The mixture was concentrated under reduced pressure and added with 5 mL of water, extracted with dichloromethane (5 mL×3). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain methyl 1-methylpyrrolidine-2-carboxylate 10c (4.7 g, yield 70.1) crude product as a brown oil.
後処理
- temperatureThe reaction mixture was warmed up to room temperature
- temperaturecooled to 0-5° C. in an ice-water bath
- temperatureThe reaction mixture was warmed up to room temperature
- stirringstirred for 24 hours
- concentrationThe mixture was concentrated under reduced pressure
- additionadded with 5 mL of water
- extractionextracted with dichloromethane (5 mL×3)
- dry with materialThe combined organic extracts were dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-a749d6dee02341f1ab6cf487c828680f
- 出典データセット
- uspto-grants-2016_06
- 特許番号
- US09358227B2
反応ノート
読み込み中…