Реакция #155403

Уравнение реакции

N-Boc-3-methylene-cyclobutanamine

K2CO3

→

N-Boc-3-amino-cyclobutanone

Выход 177.6%

Растворители

DCM

H2O

Условия реакции

Обработка

1. 1
   ДругоеDuring the course of the reaction
2. 2
   Фильтрацияupon completion, the reaction mixture was filtered through a pad of celite
3. 3
   ДругоеThe filtrates were transferred to a separatory funnel
4. 4
   Экстракцияthe aqueous layer was extracted with DCM (2×50 mL)
5. 5
   ПромывкаThe combined organic layers were washed with 5% NaHCO3 (2×30 mL), brine (30 mL)
6. 6
   Сушкаdried over Na2SO4
7. 7
   Фильтрацияfiltered
8. 8
   Другоеevaporated to dryness
9. 9
   Другоеto yield a crude, which
10. 10
    Другоеwas purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-60%)

Методика

To a vigorously stirring solution of N-Boc-3-methylene-cyclobutanamine (9.8 g, 53.5 mmol) in DCM (160 mL) and H2O (160 mL) was added K2CO3 (3 g, 21.7 mmol), followed by NaClO4 (35 g, 163.5 mmol), tetrabutylammonium chloride (0.2 g, 0.72 mmol) and RuCl3 (0.6 g, 7.6 mmol). During the course of the reaction, the organic solution turned dark brown, the catalyst turned black, while the upper aqueous layer turned white. The reaction was monitored by TLC, and upon completion, the reaction mixture was filtered through a pad of celite. The filtrates were transferred to a separatory funnel, and the aqueous layer was extracted with DCM (2×50 mL). The combined organic layers were washed with 5% NaHCO3 (2×30 mL), brine (30 mL), dried over Na2SO4, filtered and evaporated to dryness to yield a crude, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-60%) to yield the desired N-Boc-3-amino-cyclobutanone (7.13 g, 38.53 mmol, 72% yield): NMR (250 MHz, CDCl3) δ 4.88 (bs, 1H), 4.13-4.29 (m, 1H), 3.23-3.41 (m, 2H), 2.9-3.05 (m, 2H), 1.39 (s, 9H).

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