Реакция #73877

ord-c0d81d75474948ff90c80476fd5f2cab

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthen evaporated
  2. 2
    Другоеto afford a dark oil
  3. 3
    Экстракцияextracted with CH2Cl2
  4. 4
    Промывкаwashed with water (2×)
  5. 5
    Другоеevaporated to ˜100 mL
  6. 6
    workup.ADDITIONHexane (300 mL) was added
  7. 7
    Фильтрацияthe product collected by filtration

Методика

1-(4-Bromo-phenyl)-cyclopropanecarboxylic acid (22 g, 91.3 mmol) and SOCl2 (13.6 mL, 183 mmol) in CH2Cl2 were heated together for 1.5 hours then evaporated to afford a dark oil. This oil was added via syringe over 30 minutes to a mixture of MeSO2NH2 (19 g, 200 mmol) in THF (250 mL) that was pre-treated at room temperature with NaH (60% in oil; 8.0 g, 200 mmol) for 1.5 hours. After a further 20 minutes, the mixture was poured into water, acidified and extracted with CH2Cl2, washed with water (2×) and evaporated to ˜100 mL. Hexane (300 mL) was added and the product collected by filtration to yield the title compound (25 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08541587B2uspto-grants-2013_09