Реакция #161511
ord-d3c8a690dbb645429f6b758516825c7a
Уравнение реакции
Реактанты
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1КонцентрированиеAfter concentration under reduced pressure, hexanes
- 2workup.ADDITIONwas added
- 3Другоеsonicated
- 4Другоеthe precipitate was removed by filtration
- 5Промывкаthe solids washed with hexanes
- 6КонцентрированиеThe combined filtrates were concentrated under reduced pressure
- 7ДругоеPurification 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).