Реакция #1519112

ord-c6061b08edd34edfa0b94a31768227b2

Уравнение реакции

C1CCOC1
THF
O=C1N[C@@H](Cc2ccccc2)CO1
4-(S)-benzyloxazolidin-2-one
[Li][CH2]CCC
n-BuLi
CCCCCC
hexane
C1CCOC1
THF
CCCCCC(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
N-hexanoyl-4-(S)-benzyloxazolidin-2-one

Условия реакции

Температура
-78°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe mixture is stirred at −78° C. for 2 hours
  2. 2
    Температураto warm to rt
  3. 3
    workup.STIRRINGstirred overnight
  4. 4
    ДругоеThe reaction is then quenched with aqueous saturated NH4Cl
  5. 5
    Экстракцияextracted with EtOAc
  6. 6
    Другоеdried
  7. 7
    Другоеpurified by silica gel chromatography (hexanes/EtOAc)

Методика

To a solution of 4-(S)-benzyloxazolidin-2-one (56 mmol) (Aldrich, Milwaukee, Wis.) in THF at −78° C. is added 2.5 M n-BuLi in hexane (22:4 mL, 56 mmol) and the reaction is stirred at −78° C. for 2 hours. To this is added via cannula a −78° C. solution of acid chloride A-1 (R=hexanoyl, 65 mmol) in THF and the mixture is stirred at −78° C. for 2 hours, then allowed to warm to rt and stirred overnight. The reaction is then quenched with aqueous saturated NH4Cl, extracted with EtOAc, dried and purified by silica gel chromatography (hexanes/EtOAc) to afford N-hexanoyl-4-(S)-benzyloxazolidin-2-one (A-2).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07612059B2uspto-grants-2009_11