Réaction #1340600

Équation de réaction

methyllithium

diethyl ether

(3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-(p-toluenesulfonyloxy)methylpyrrolidine

diethyl ether

ammonium chloride

ammonia

→

title compound

(3S,4S)-1-Benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-ethylpyrrolidine

Solvants

water

Conditions de réaction

Traitement

1. 1
   TempératureUnder cooling with ice
2. 2
   workup.STIRRINGby stirring for 1 hour
3. 3
   Températureunder cooling with ice
4. 4
   TempératureUnder cooling with ice
5. 5
   Extractionfollowed by extraction with ethyl acetate (300 mL×2)
6. 6
   LavageThe combined organic layer was washed by saturated brine (100 mL)
7. 7
   Séchagedried over anhydrous sodium sulfate
8. 8
   ConcentrationThe filtrate was concentrated under reduced pressure
9. 9
   AutreThe residue was purified through silica gel column chromatography (ethyl acetate:n-hexane=1:3 to 1:2)

Mode opératoire

Under cooling with ice, a solution of methyllithium (121 mL, 1.02 M, diethyl ether solution) was added to a suspension of copper(I) iodide (11.8 g, 62.1 mmol) in diethyl ether (200 mL), followed by stirring for 30 minutes. The temperature of the reaction mixture was cooled to −78° C. A solution of (3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-(p-toluenesulfonyloxy)methylpyrrolidine (6.27 g, 12.4 mmol) in diethyl ether (140 mL) was added thereto. The temperature of the mixture was elevated gradually, followed by stirring for 1 hour under cooling with ice. Under cooling with ice, a saturated aqueous ammonium chloride solution (100 mL) and 28% aqueous ammonia (25 mL) were added to the resultant mixture, and then water (100 mL) was added thereto, followed by extraction with ethyl acetate (300 mL×2). The combined organic layer was washed by saturated brine (100 mL), and dried over anhydrous sodium sulfate. The filtrate was concentrated under reduced pressure. The residue was purified through silica gel column chromatography (ethyl acetate:n-hexane=1:3 to 1:2), to thereby yield the title compound as a colorless oily substance (3.09 g, 71%).

Source