Methyl iodide → Methyl α-propoxy-1H-indole-5-propanoate

反応式

[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH2:10][CH:11]([O:15][CH2:16][CH2:17][CH3:18])[C:12]([OH:14])=[O:13])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[C:19](=O)([O-])O.[Na+].CI>CN(C)C=O>[CH3:19][O:13][C:12](=[O:14])[CH:11]([O:15][CH2:16][CH2:17][CH3:18])[CH2:10][C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][CH:2]=[CH:3]2

参加物

実験手順

Crude rac-3-(1H-indol-5-yl)-2-propoxy-propionic acid was dissolved in 5 ml N,N-dimethylformamide, 0.54 g of sodium hydrogencarbonate was added followed by 0.32 nm of methyl iodide. The mixture was stirred at r.t. for 7 hours, then poured into ice water and extracted 3 times with ethyl acetate; after drying over MgSO4 and evaporation, the crude product was purified by chromatograph) (silicagel, eluent: gradient of n-heptane/ethyl acetate) to yield 0.47 g of rac-3-(1H-indol-5-yl)-2-propoxy-propionic acid methyl ester as light yellow oil.