Methyl(6-phenoxy-2-pyridyl)methanol → Methyl[6-(4-fluorophenoxy)-2-pyridyl]methyl 2-(2-naphthyl)-3-methylbutanoate
反応式
CC(C1C=CC=C(OC2C=CC=CC=2)N=1)O.[CH3:17][CH:18]([C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([O:26][C:27]2[CH:32]=[CH:31][C:30]([F:33])=[CH:29][CH:28]=2)[N:21]=1)[OH:19].[CH:34]1[C:43]2[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:37]=[CH:36][C:35]=1[CH:44]([CH:48]([CH3:50])[CH3:49])[C:45](O)=[O:46]>>[CH:34]1[C:43]2[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:37]=[CH:36][C:35]=1[CH:44]([CH:48]([CH3:50])[CH3:49])[C:45]([O:19][CH:18]([CH3:17])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([O:26][C:27]2[CH:32]=[CH:31][C:30]([F:33])=[CH:29][CH:28]=2)[N:21]=1)=[O:46]参加物
4
実験手順
Following the procedure of Example 3, each of methyl (6-phenoxy-2-pyridyl)methanol and methyl[6-(4-fluorophenoxy)-2-pyridyl]methanol is reacted with 2-(2-naphthyl)-3-methyl-butanoic acid to yield methyl (6-phenoxy-2-pyridyl) methyl 2-(2-naphthyl)-3-methylbutanoate and methyl[6-(4-fluorophenoxy)-2-pyridyl]methyl 2-(2-naphthyl)-3-methylbutanoate, respectively.