Реакция #1552042

ord-851fa221374449539c464633e72a3034

Уравнение реакции

CC(=O)N[C@@H](Cc1ccccc1)C(=O)OCC[Se]c1ccccc1
N-acetylphenylalanine 2-(phenylseleno)ethyl ester
OO
H2O2
C=COC(=O)[C@H](Cc1ccccc1)NC(C)=O
N-acetylphenylalanine vinyl ester

Реагенты

Нет

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGAfter stirring the mixture for 12 hours at room temperature
  2. 2
    Экстракцияextracted with 3×50 ml of water
  3. 3
    СушкаThe organic phases were then dried over sodium sulfate
  4. 4
    Другоеthe solvent was removed
  5. 5
    Температураwas refluxed for 24 hours
  6. 6
    ТемператураAfter cooling
  7. 7
    Другоеthe solvent was removed
  8. 8
    ДругоеFlash column—chromatography (PE:EE=3:1) yielded 1.3 g (84% of th., 93% of lit.) of a light-yellow liquid

Методика

To a solution of 2.6 g (6.66 mmol) of N-acetylphenylalanine 2-(phenylseleno)ethyl ester in 20 ml of THF, 8 ml of a 30% H2O2 solution were added dropwise within 10 minutes at 0° C., and the solution was stirred at 0° C. for another 30 minutes. After stirring the mixture for 12 hours at room temperature, it was diluted with 80 ml of CHCl3 and extracted with 3×50 ml of water. The organic phases were then dried over sodium sulfate, and the solvent was removed. The residue was taken up in 70 ml of chloroform and was refluxed for 24 hours. After cooling, the solvent was removed. Flash column—chromatography (PE:EE=3:1) yielded 1.3 g (84% of th., 93% of lit.) of a light-yellow liquid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08999323B2uspto-grants-2015_04