4-(Bromomethyl)phenylacetic acid → 2-[4-(Aminomethyl)phenyl]ethan-1-ol
反応式
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]([OH:12])=O)=[CH:5][CH:4]=1.[NH3:13].CCO>>[NH2:13][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][OH:12])=[CH:5][CH:4]=1参加物
反応条件
- 温度
- 70 °C
実験手順
To a stirred solution of NH3/EtOH (170 mL) was added (4-Bromomethyl-phenyl)-acetic acid (1.61 g, 7.01 mmol). The resultant solution was stirred at room temperature for 2 h. The mixture was concentrated in vacuo, and redissolved with anhydrous THF (10 mL). To the solution, BH3.Me2S was added, and the mixture was stirred for 1 h at 70° C., and at room temperature for 2 d. The reaction was concentrated in vacuo, 6 N HCl (10 mL) was added, and the mixture was stirred at 70° C. for 1 h. Water (20 mL) was added, and it was neutralized with 1 N NaOH to pH˜7. The solution was concentrated to dryness under high vacuum, washed with MeOH/CH2Cl2, and filtered. The crude product was purified by flash chromatography on silica gel (5:3:92 CH3OH—NH3 H2O—CH2Cl2) to afford the title compound (820 mg, 77%) as a white foam.
後処理
- concentrationThe mixture was concentrated in vacuo
- dissolutionredissolved with anhydrous THF (10 mL)
- additionMe2S was added
- waitat room temperature for 2 d
- concentrationThe reaction was concentrated in vacuo, 6 N HCl (10 mL)
- additionwas added
- stirringthe mixture was stirred at 70° C. for 1 h
- additionWater (20 mL) was added
- concentrationThe solution was concentrated to dryness under high vacuum
- washwashed with MeOH/CH2Cl2
- filtrationfiltered
- customThe crude product was purified by flash chromatography on silica gel (5:3:92 CH3OH—NH3 H2O—CH2Cl2)
出典と根拠
- ORDレコード
- ord-f39523ae1dee437e8037402bd661af82
- 出典データセット
- uspto-grants-2007_12
- 特許番号
- US07312234B2
反応ノート
読み込み中…