Benzylethanolamine → Ethyl (4-benzylmorpholin-2-yl)acetate
反応式
[CH2:1]([NH:8][CH2:9][CH2:10][OH:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.Br[CH2:20]/[CH:21]=[CH:22]/[C:23]([O:25][CH2:26][CH3:27])=[O:24].[OH-].[Na+]>C(OCC)(=O)C.O>[CH2:1]([N:8]1[CH2:9][CH2:10][O:11][CH:21]([CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:20]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 25 °C
実験手順
2-(Benzylamino)ethanol (19.05 ml, 132 mmol) and triethylamine (18.44 ml, 132 mmol) was added to water (150 ml) and the resulting mixture was heated to reflux temperature. (E)-Ethyl 4-bromobut-2-enoate (18.24 ml, 132 mmol) was added dropwise for 10 min The resulting mixture was further maintained at reflux temperature for 5 h. The reaction mixture was cooled to 25° C. and added NaOH (5.29 g, 132 mmol) after that the solvent was removed by distillation under reduced pressure to give orange oil. Ethyl acetate (150 mL) was added and the resulting solution was washed with water (2×50 mL). Ethyl acetate was distilled off under reduced pressure to give crude compound (15 g). This crude compound was purified by flash chromatography (Biotage) using eluent 20% ethyl acetate in hexane to yield 13 g of pure title compound as colorless viscous oil. m/z 264.08.
後処理
- temperaturethe resulting mixture was heated
- temperatureto reflux temperature
- temperaturewas further maintained
- temperatureat reflux temperature for 5 h
- customwas removed by distillation under reduced pressure
- customto give orange oil
- washthe resulting solution was washed with water (2×50 mL)
- distillationEthyl acetate was distilled off under reduced pressure
- customto give crude compound (15 g)
- customThis crude compound was purified by flash chromatography (Biotage)
出典と根拠
- ORDレコード
- ord-a78af227dd354035adb7a0f759ac4a99
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09382216B2
反応ノート
読み込み中…