反応式
[CH3:1][O:2][C:3](=[O:18])[C:4](=[CH:10][C:11]1[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=1)[CH:5]([CH3:9])[C:6]([OH:8])=O.COC(C1C=C(O)C2C(=CC=C(F)C=2)C=1)=O>>[CH3:1][O:2][C:3]([C:4]1[C:5]([CH3:9])=[C:6]([OH:8])[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([F:17])[CH:15]=2)[CH:10]=1)=[O:18]参加物
3
実験手順
Alternatively, Starting with 2-(4-fluoro-benzylidene)-3-methyl-succinic acid 1-methyl ester, using a method analogous to the one described above for 6-fluoro-4-hydroxy-naphthalene-2-carboxylic acid methyl ester, 6-fluoro-4-hydroxy-3-methyl-naphthalene-2-carboxylic acid methyl ester was obtained as a pale solid.
出典と根拠
- ORDレコード
- ord-09f9221f91c1416bacfd5a53a902d297
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08188090B2
関連ノート
読み込み中…