Реакция #11844

ord-5f42e2530e154a3096b9b9ddf20e8732

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONafter the addition
  2. 2
    Экстракцияextracted with ethyl acetate (3×80 mL)
  3. 3
    ЭкстракцияThe combined extract
  4. 4
    Промывкаwas washed sequentially with water (80 mL), and brine (80 mL)
  5. 5
    Сушкаdried (MgSO4)
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеfinally concentrated

Методика

PBr3 (2.4 mL. 25.8 mmol) was added dropwise at 0° C. under nitrogen to a stirred solution of tert-butyl 4-(hydroxymethyl) 1H-1-indolecarboxylate 6 (6.0 g, 24.3 mmol) in ether (80 mL) and CH2Cl2 (20 mL) under nitrogen. The reaction was completed 30 minutes after the addition. The mixture was poured into a cold aqueous NaHCO3 solution (100 mL) and extracted with ethyl acetate (3×80 mL). The combined extract was washed sequentially with water (80 mL), and brine (80 mL), then dried (MgSO4), filtered, and finally concentrated to provide tert-butyl 4-(bromomethyl)-1H-1-indolecarboxylate 7 (6.3 g, 84%) as an oil which was immediately taken to the next step.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07098307B2uspto-grants-2006_08