Реакция #1864

ord-81f17a5f0c63408184ecd6ae2c164668

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe mixture was quenched with aq. Na2 CO3 and aq. NaHCO3 until basic at 0° C
  2. 2
    ДругоеThe organic layer was dried
  3. 3
    Другоеevaporated to a foam (10 g)

Методика

cis-(±)-5-Bromo-1,2,3,3a,8,8a-hexahydro-6-methoxy- 1,3a,8-trimethyl-pyrrolo[2,3-b]indole (11 g) was dissolved in dry DCM (200 ml) and added dropwise at 0° C. to a stirred solution of BBr3 in DCM (300 ml). The mixture was warmed to room temperature and stirred overnight under nitrogen. The mixture was quenched with aq. Na2 CO3 and aq. NaHCO3 until basic at 0° C. The organic layer was dried and evaporated to a foam (10 g). The IR, NMR and Mass Spectra confirmed the purity and identity of this product.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726323uspto-grants-1998_03