反応 #11537

反応方程式

bromoacetic acid

Propylamine

di-t-butyl carbonate

citric acid monohydrate

sodium hydroxide

→

2-[N-(t-butoxycarbonyl)-N-propylamino]acetic acid

収率 65.0%

溶媒

Ethanol

tetrahydrofuran

反応条件

後処理

1. 1
   温度cooling
2. 2
   workup.STIRRINGthe whole was stirred at an external temperature of 80° C. for 2.5 hours
3. 3
   濃縮the whole was concentrated under reduced pressure
4. 4
   workup.ADDITIONThen, water (27 ml) and tetrahydrofuran (30 ml) were added to the concentrate
5. 5
   workup.STIRRINGthe mixture was stirred at room temperature
6. 6
   抽出The whole was extracted with ethyl acetate (150 ml)
7. 7
   洗浄the organic layer was washed with water (100 ml) and saturated brine (50 ml) successively
8. 8
   乾燥The organic layer was dried over sodium sulfate
9. 9
   濃縮concentrated under reduced pressure
10. 10
    その他The residue was purified by silica gel column chromatography

実験手順

Ethanol (36 ml) was added to bromoacetic acid (5.00 g, 36.0 mmol), and the mixture was stirred under ice-cold water-cooling. Propylamine (14.8 ml, 180 mmol) was added to the mixture over one minute, and then the whole was stirred at an external temperature of 80° C. for 2.5 hours. A 4 N aqueous sodium hydroxide solution (27 ml) was added thereto, and the whole was concentrated under reduced pressure. Then, water (27 ml) and tetrahydrofuran (30 ml) were added to the concentrate, and the mixture was stirred at room temperature. A solution of di-t-butyl carbonate (9.43 g, 43.2 mmol) in tetrahydrofuran (6 ml) was added to the mixture, and after 15 minutes, citric acid monohydrate was added to the reaction mixture to acidify it weakly. The whole was extracted with ethyl acetate (150 ml), and the organic layer was washed with water (100 ml) and saturated brine (50 ml) successively. The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 5.06 g (65%) of 2-[N-(t-butoxycarbonyl)-N-propylamino]acetic acid as a colorless solid.

出典