Реакция #44469
ord-bac32aa16a0143ae82d270190b816ba0
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ФильтрацияAfter filtration through dicalite
- 2Промывкаwashing with CH2Cl2
- 3Другоеthe volatiles were removed in vacuo
- 4workup.DISSOLUTIONThe crude product was dissolved in ethanol (250 mL) wherafter 2N (aq) NaOH (20 mL)
- 5workup.ADDITIONwas added
- 6workup.STIRRINGThis mixture was stirred at room temperature for 2.5 h
- 7ФильтрацияThe reaction mixture was filtrated through dicalite
- 8Промывкаwashed with CH2Cl2
- 9ДругоеAfter removal of the solvent under reduced pressure
- 10workup.DISSOLUTIONthe residu was dissolved in ethanol (350 mL)
- 11workup.ADDITIONNaOH (2N, 20 mL) was added
- 12workup.STIRRINGthe mixture was stirred for 3 h
- 13workup.ADDITIONWater was added
- 14Экстракцияthe mixture was extracted with ethyl acetate (3×)
- 15ПромывкаThe combined organic layers were washed with brine
- 16Другоеdried
- 17Другоеevaporated
Методика
To a solution of 8-chloro-10,11-dihydro-5H-dibenzo[b,f][1,4]diazepine (8.75 g, 37.9 mmol) in CH2Cl2 (375 mL) was added MnO2 (14.5 g, 166 mmol). The reaction mixture was stirred at room temperature for 1.5 h. After filtration through dicalite, washing with CH2Cl2, the volatiles were removed in vacuo. The crude product was dissolved in ethanol (250 mL) wherafter 2N (aq) NaOH (20 mL) was added. This mixture was stirred at room temperature for 2.5 h. The reaction mixture was filtrated through dicalite and washed with CH2Cl2. After removal of the solvent under reduced pressure, the residu was dissolved in ethanol (350 mL). NaOH (2N, 20 mL) was added and the mixture was stirred for 3 h. Water was added and the mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried and evaporated to afford the title compound (8.9 g, 38.9 mmol).