3-(3,4-Dimethoxyphenyl)-4,4-diethoxy-2-ethoxycarbonylbutyric acid ethyl ester → 4,4-Diethoxy-3-[3-(2-ethylbutoxy)-4-methoxyphenyl] butyric acid
반응식
C([O:3][C:4](=[O:34])[CH:5](C(OCC)=O)[CH:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([O:22][CH2:23][CH:24]([CH2:27][CH3:28])[CH2:25][CH3:26])[CH:15]=1)[CH:7]([O:11][CH2:12][CH3:13])[O:8][CH2:9][CH3:10])C.C(OC(=O)C(C(OCC)=O)C(C1C=CC(OC)=C(OC)C=1)C(OCC)OCC)C>>[CH2:9]([O:8][CH:7]([O:11][CH2:12][CH3:13])[CH:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([O:22][CH2:23][CH:24]([CH2:27][CH3:28])[CH2:25][CH3:26])[CH:15]=1)[CH2:5][C:4]([OH:34])=[O:3])[CH3:10]참가 물질
3
실험 절차
Using the same procedure as in Example 1(3), 4,4-diethoxy-2-ethoxycarbonyl-3-[3-(2-ethylbutoxy)-4-methoxyphenyl]butyric acid ethyl ester, instead of 3-(3,4-dimethoxyphenyl)-4,4-diethoxy-2-ethoxycarbonylbutyric acid ethyl ester, was used to obtain a yellow solid of the above-described compound via 4,4-diethoxy-3-[3-(2-ethylbutoxy)-4-methoxyphenyl] butyric acid (yield 36.9%).