Реакция #161511

ord-d3c8a690dbb645429f6b758516825c7a

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAfter concentration under reduced pressure, hexanes
  2. 2
    workup.ADDITIONwas added
  3. 3
    Другоеsonicated
  4. 4
    Другоеthe precipitate was removed by filtration
  5. 5
    Промывкаthe solids washed with hexanes
  6. 6
    КонцентрированиеThe combined filtrates were concentrated under reduced pressure
  7. 7
    ДругоеPurification by flash chromatography (10 to 50% EtOAc-hexanes gradient)

Методика

Cycloheptylmethanol was coupled with 3-bromophenol following the method used in Example 10. After concentration under reduced pressure, hexanes was added. The mixture was stirred and sonicated then the precipitate was removed by filtration and the solids washed with hexanes. The combined filtrates were concentrated under reduced pressure. Purification by flash chromatography (10 to 50% EtOAc-hexanes gradient) gave ((3-bromophenoxy)methyl)cycloheptane. (Yield 1.0697 g, 56%): 1H NMR (400 MHz, CDCl3) δ 7.12 (t, J=8.4, 1H), 7.06-7.04 (m, 2H), 6.82 (dq, J=8.0, 1.2, 1H), 3.70 (d, J=6.4, 2H), 1.91-1.98 (m, 1H), 1.81-1.88 (m, 2H), 1.42-1.72 (m, 8H), 1.24-1.34 (m, 2H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08829244B2uspto-grants-2014_09