反応式
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([O:11][CH3:12])[CH:3]=1.S(Cl)(Cl)=O.[CH3:17]O>>[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH3:17])=[O:7])=[C:4]([O:11][CH3:12])[CH:3]=1参加物
4
実験手順
To a solution of 4-fluoro-2-methoxybenzoic acid (1.7 g, 10 mmol) in methanol (100 mL) was added thionyl chloride (5.73 g, 48 mmol) at 0° C. The resultant mixture was stirred for 12 hours and then solvent was evaporated in vacuo. To the residue, saturated sodium bicarbonate aqueous solution (50 mL) was added and the mixture was extracted with ethyl acetate (100 mL×3). The organic phase was dried by sodium sulfate. The mixture was filtered and the filtrate was concentrated in vacuo to give methyl 4-fluoro-2-methoxybenzoate (1.3 g, 70%).
後処理
- customsolvent was evaporated in vacuo
- additionTo the residue, saturated sodium bicarbonate aqueous solution (50 mL) was added
- extractionthe mixture was extracted with ethyl acetate (100 mL×3)
- dry with materialThe organic phase was dried by sodium sulfate
- filtrationThe mixture was filtered
- concentrationthe filtrate was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-167e5eb73039453588418454e438bb0b
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09206128B2
関連ノート
読み込み中…