Реакция #77178

ord-3f77a10e74bf44d4b323cf8ea0e05ff6

Уравнение реакции

O=C(O)CCCCCCCBr
8-bromooctanoic acid
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
OCc1ccccc1
benzyl alcohol
O=C(CCCCCCCBr)OCc1ccccc1
Benzyl-8-bromoctanoate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe precipitation of the expected dicyclohexylurea (DCU)
  2. 2
    Другоеto come back to room temperature
  3. 3
    workup.WAITThen after about 1 hr
  4. 4
    workup.ADDITION0.5 ml of AcOH were added
  5. 5
    Другоеto quench
  6. 6
    Фильтрацияthe DCU was filtered out after about one hour (yield 11.2 g=100%)

Методика

There were dissolved 11.6 g (52 mmol) of 8-bromooctanoic acid in 100 ml of CCl4 and around 5° C. (ice bath), there were added to the solution 5.41 g (50 mmol) of benzyl alcohol and 2.5 mmol of 4-pyrrolidino-pyridine catalyst. Thereafter, a solution of 10.73 g (52 mmol) of dicyclohexylcarbodiimide (DCC) in 10 ml of carbon tetrachloride was added portion-wise under stirring. The precipitation of the expected dicyclohexylurea (DCU) was effective after a few min and the temperature was allowed to come back to room temperature. After ½ hr, the reaction was complete as checked by TLC (hexane/ether 1:1). Then after about 1 hr, 0.5 ml of AcOH were added to quench remaining DCC and the DCU was filtered out after about one hour (yield 11.2 g=100%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06706280B2uspto-grants-2004_03