Nitrous Acid → Methyl 4-fluoro-2-phenylbenzoate
反応式
N[C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:3]=1.N([O-])=O.[Na+].N(O)=O.[H+].[B-](F)(F)(F)[F:27]>>[CH3:9][O:8][C:6](=[O:7])[C:5]1[CH:10]=[CH:11][C:2]([F:27])=[CH:3][C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
5
実験手順
A solution of methyl 4-amino-2-phenylbenzoate (1.0 equivalent) in dilute aqueous HBF4 is treated with NaNO2 (1.1 equivalents) until an excess of nitrous acid persists. The mixture is extracted into ethyl acetate which is dried and evaporated. The title ester is purified by chromatography on silica gel.
後処理
- extractionThe mixture is extracted into ethyl acetate which
- customis dried
- customevaporated
- customThe title ester is purified by chromatography on silica gel
出典と根拠
- ORDレコード
- ord-3051e44a821e4ec2913cf33f4e271308
- 出典データセット
- uspto-grants-2001_03
- 特許番号
- US06204293B1
反応ノート
読み込み中…