Реакция #1173

ord-d13c6a79a6d1480ca22e3b132fc186d6

Уравнение реакции

O=C1NC(=O)c2ccccc21
phthalimide
O=C(OCc1ccccc1)N1CCCCC1
N-Cbz-piperidine
CCOC(=O)/N=N/C(=O)OCC
DEAD
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
O=C(OCc1ccccc1)N1CCC(N2C(=O)c3ccccc3C2=O)CC1
1-benzyloxycarbonyl-4-phthalimidylpiperidine
Выход 50.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas quenched with water
  2. 2
    Экстракцияextracted with EtOAc (3×)
  3. 3
    Промывкаthe combined extracts washed with brine solution
  4. 4
    Сушкаdried over Na2SO4
  5. 5
    Концентрированиеconcentrated
  6. 6
    Другоеto give the crude product
  7. 7
    ДругоеPurification of this material by chromatography (hexanes/EtOAc; 2:1)

Методика

A solution of DEAD (1.61 mL, 10.2 mmol) in 20 mL of THF was added to a solution of triphenylphosphine (2.69 g, 10.3 mmol), the N-Cbz-piperidine prepared in Example 16A (2.36 g, 100 mmol) and phthalimide (1.50 g, 10.2 mmol) in 80 mL of THF. After stirring 10.5 h at R.T. the mixture was quenched with water, extracted with EtOAc (3×) and the combined extracts washed with brine solution, dried over Na2SO4 and concentrated to give the crude product. Purification of this material by chromatography (hexanes/EtOAc; 2:1) gave 1.81 g, (50%) of 1-benzyloxycarbonyl-4-phthalimidylpiperidine. [1H]-NMR(CDCl3) consistent with structure.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723490uspto-grants-1998_03