Реакция #51755

ord-7912b342b8fa4b6881975c0f1349c2c5

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas cooled to 0° C.
  2. 2
    ДругоеThe solvents were evaporated
  3. 3
    workup.DISSOLUTIONthe residue was dissolved in EtOAc
  4. 4
    Промывкаwashed with saturated NaHCO3 solution and brine
  5. 5
    Другоеdried
  6. 6
    Концентрирование(MgSO4.) Concentration

Методика

6-tert-Butyl-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (Prepared in Example HH; 12.0 g) in CH2Cl2 (100 mL) was cooled to 0° C. and treated with HCl gas for 10 minutes. The reaction mixture was warmed to room temperature and stirred for 1 hour. The solvents were evaporated; the residue was dissolved in EtOAc, washed with saturated NaHCO3 solution and brine, and dried (MgSO4.) Concentration gave the title compound which was used without any further purification. MS(APCI): 176 (M+H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06852711B2uspto-grants-2005_02