Реакция #1005945
ord-b33c518d2e2b468c98a400ed6f9f302f
Уравнение реакции
sodium carbonate
t-butyl {4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-pyrrolidin-1-yl]-2-(trifluoromethyl)benzyl}carbamate
hydrochloric acid
ethanol
→
title compound
Выход 105.6%
1-{4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-pyrrolidin-1-yl]-2-(trifluoromethyl)phenyl}methanamine
Выход 105.6%
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1workup.ADDITIONthe reaction solution was diluted
- 2ЭкстракцияAfter the extraction
- 3Промывкаthe organic layer was washed with saturated brine
- 4Сушкаdried over anhydrous magnesium sulfate
- 5ДругоеThe solvent was evaporated off under reduced pressure
Методика
A mixture comprising t-butyl {4-[3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-pyrrolidin-1-yl]-2-(trifluoromethyl)benzyl}carbamate (6.0 g), concentrated hydrochloric acid (20 mL) and ethanol (100 mL) was stirred at 50° C. for three hours. After cooling the mixture to room temperature, the reaction solution was diluted by adding water (150 mL) and ethyl acetate (150 mL). By adding sodium carbonate in small portions, the solution was neutralized. After the extraction using ethyl acetate, the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated off under reduced pressure to obtain the title compound (5.2 g).