Diethyl Oxalate → Ethyl 4-oxo-8-[(E)-2-[4-(4-phenylbutoxy)phenyl]-ethen-1-yl]-4H-1-benzopyran-2-carboxylate
반응식
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:17]=[CH:16][C:15](/[CH:18]=[CH:19]/[C:20]3[C:21]([OH:29])=[C:22]([C:26](=[O:28])[CH3:27])[CH:23]=[CH:24][CH:25]=3)=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:30](OCC)(=O)[C:31]([O:33][CH2:34][CH3:35])=[O:32]>>[O:28]=[C:26]1[C:22]2[CH:23]=[CH:24][CH:25]=[C:20](/[CH:19]=[CH:18]/[C:15]3[CH:16]=[CH:17][C:12]([O:11][CH2:10][CH2:9][CH2:8][CH2:7][C:1]4[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=4)=[CH:13][CH:14]=3)[C:21]=2[O:29][C:30]([C:31]([O:33][CH2:34][CH3:35])=[O:32])=[CH:27]1참가 물질
3
실험 절차
Following the process described in example 1 (point A), starting from 3'-[(E)-2-[4-(4-phenylbutoxy)phenyl]-ethen-1-yl]-2'-hydroxyacetophenone and diethyl oxalate, the title compound was prepared, which was purified by chromatography through a silica gel column, eluting with petroleum ether:chloroform, 6:4 (66% yield).
후처리
- customwhich was purified by chromatography through a silica gel column
- wash