Ethanol → ethyl 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetate

反応式

[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[C:6]2[C:12](=[O:16])[C:13](Cl)=[O:14].CCN(CC)CC.[CH2:24]([OH:26])[CH3:25]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]=[C:6]2[C:12](=[O:16])[C:13]([O:26][CH2:24][CH3:25])=[O:14]

参加物

反応物 3

HCID 702Ethanol

HCID 8471Triethylamine

HCID 99917662-(5-methoxy-1H-indol-3-yl)-2-oxoacetyl chloride

生成物 1

HCID 2763354ethyl 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetate

実験手順

To a solution 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetyl chloride (14.78 g, 62.20 mmol) in ethanol (144 mL), Et3N (10.40 mL, 74.63 mmol) was added at 0° C. and the resulting yellow suspension was stirred at rt for 1 h. The percipitate was filtered off, washed with cold ethanol and diethylether to yield ethyl 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetate as an orange oil. LC-MS conditions B: tR=0.63 min, [M+H]+=248.13.