تفاعل #511784
ord-bdadca84664a4d8faf9ff13b5cd20f82
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزThe reaction mixture was concentrated under reduced pressure
- 2workup.DISSOLUTIONthe residue was dissolved in ethyl acetate (200 ml)
- 3غسيلThe solution was washed with water (50 ml), 5% citric acid aqueous solution (50 ml×twice), saturated brine (50 ml), 5% sodium hydrogencarbonate aqueous solution (50 ml×twice), and saturated brine (50 ml)
- 4تجفيفThe organic layer was dried over anhydrous magnesium sulfate
- 5أخرىthe magnesium sulfate was removed by filtration
- 6تركيزthe filtrate was concentrated under reduced pressure
- 7أخرىThe residue was recrystallized from ethyl acetate/n-hexane
الإجراء التجريبي
Boc-Val-OH (8.69 g, 40.0 mmol) and Gly-OBzl.HCl (8.07 g, 40.0 mmol) were dissolved in methylene chloride (100 ml), and the solution was maintained at 0° C. Triethylamine (6.13 ml, 44.0 mmol), HOBt (1-hydroxybenzotriazole, 6.74 g, 44.0 mmol), and WSC.HCl (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, 8.44 g, 44.0 mmol) were added to the solution, and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate (200 ml). The solution was washed with water (50 ml), 5% citric acid aqueous solution (50 ml×twice), saturated brine (50 ml), 5% sodium hydrogencarbonate aqueous solution (50 ml×twice), and saturated brine (50 ml). The organic layer was dried over anhydrous magnesium sulfate, then the magnesium sulfate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/n-hexane to obtain white crystals of Boc-Val-Gly-OBzl (13.2 g, 36.2 mmol).