Réaction #66402

Équation de réaction

N-Boc-3-methylene-cyclobutanamine

K2CO3

→

N-Boc-3-amino-cyclobutanone

Rendement 177.6%

Solvants

DCM

H2O

Conditions de réaction

Traitement

1. 1
   AutreDuring the course of the reaction
2. 2
   Filtrationupon completion, the reaction mixture was filtered through a pad of celite
3. 3
   AutreThe filtrates were transferred to a separatory funnel
4. 4
   Extractionthe aqueous layer was extracted with DCM (2×50 mL)
5. 5
   LavageThe combined organic layers were washed with 5% NaHCO3 (2×30 mL), brine (30 mL)
6. 6
   Séchagedried over Na2SO4
7. 7
   Filtrationfiltered
8. 8
   Autreevaporated to dryness
9. 9
   Autreto yield a crude, which
10. 10
    Autrewas purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-60%)

Mode opératoire

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 NaIO4 (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):

Source