3-Methyl-2-(naphthalen-2-yl)butanoic acid → (6-Benzyl-2-pyridyl)methyl 2-(2-naphthyl)-3-methylbutanoate
反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]([CH:15]([CH3:17])[CH3:16])[C:12]([OH:14])=[O:13].[CH2:18]([C:25]1[N:30]=[C:29]([CH2:31]O)[CH:28]=[CH:27][CH:26]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]([CH:15]([CH3:17])[CH3:16])[C:12]([O:14][CH2:31][C:29]1[CH:28]=[CH:27][CH:26]=[C:25]([CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:30]=1)=[O:13]参加物
3
実験手順
Following the procedure of Example 1, the acid chloride of 2-(2-naphthyl)-3-methylbutanoic acid is reacted with (6-benzyl-2-pyridyl)methanol to yield (6-benzyl-2-pyridyl)methyl 2-(2-naphthyl)-3-methylbutanoate.
出典と根拠
- ORDレコード
- ord-d14515fd88f04a3fb87b3bb471c4044c
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04223033
反応ノート
読み込み中…