Реакция #7285

Уравнение реакции

2-[N-(t-butyloxycarbonyl)]amino-cyclohexanone

aniline

acetic acid

NaBH(OAc)3

→

cis-N-phenyl-N′-(t-butyloxycarbonyl)-cyclohexane-1,2-diamine

Выход 9.0%

Растворители

CH2Cl2

THF

Условия реакции

Обработка

1. 1
   Другоеovernight
2. 2
   Промывкаwashed with saturated aqueous NaHCO3 (50 mL)
3. 3
   ПромывкаThe aqueous phase was washed with CH2Cl2 (2×25 mL)
4. 4
   Сушкаthe combined organic extracts dried (Na2SO4)
5. 5
   Фильтрацияfiltered
6. 6
   Концентрированиеconcentrated under reduced pressure
7. 7
   ДругоеPurification and separation of the resultant brown oil by flash chromatography on silica gel (Hexanes/EtOAc, 9:1)

Методика

To a solution of 2-[N-(t-butyloxycarbonyl)]amino-cyclohexanone (0.785 g, 3.69 mmol, aniline (0.68 mL, 7.46 mmol) and glacial acetic acid (0.22 mL) in THF (10 mL) was added NaBH(OAc)3 (1.173 g, 5.53 mmol) and the mixture was stirred at 60□ C. overnight. The reaction was cooled to room temperature, diluted with CH2Cl2 (60 mL) and washed with saturated aqueous NaHCO3 (50 mL). The aqueous phase was washed with CH2Cl2 (2×25 mL) and the combined organic extracts dried (Na2SO4), filtered and concentrated under reduced pressure. Purification and separation of the resultant brown oil by flash chromatography on silica gel (Hexanes/EtOAc, 9:1) afforded the low polarity cis-N-phenyl-N′-(t-butyloxycarbonyl)-cyclohexane-1,2-diamine isomer (0.095 g, 9%) and the high polarity trans-N-phenyl-N′-(t-butyloxycarbonyl)-cyclohexane-1,2-diamine isomer (0.412 g, 39%), both as pale yellow solids.

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