反应 #1340606
ord-769fa2b046694926a4ebc77edee1f8c6
反应方程式
diazomethane
(3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine
→
title compound
(3S,4S)-1-Benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-cyclopropylpyrrolidine
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1workup.ADDITIONwas added
- 2其他After completion of reaction, insoluble matter
- 3其他was removed through filtration
- 4浓缩The filtrate was concentrated under reduced pressure
- 5其他the obtained residue was purified though silica gel column chromatography (ethyl acetate:n-hexane=1:9 to 1:4)
实验过程
An excessive amount of a solution of diazomethane in diethyl ether (30 mL) was added to (3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine (270 mg, 779 μmol). Under cooling with ice, palladium acetate (10 mg) was added thereto, followed by stirring at room temperature for 2 hours. After completion of reaction, insoluble matter was removed through filtration. The filtrate was concentrated under reduced pressure, and the obtained residue was purified though silica gel column chromatography (ethyl acetate:n-hexane=1:9 to 1:4), to thereby yield the title compound as a colorless oily substance (269 mg, 96%).