Methyl chloroformate → 2-Chloro-4-fluoro-methoxycarbonyloxybenzene
反応式
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[OH:9].[OH-].[Na+].Cl[C:13]([O:15][CH3:16])=[O:14]>O>[C:13](=[O:14])([O:9][C:3]1[CH:4]=[CH:5][C:6]([F:8])=[CH:7][C:2]=1[Cl:1])[O:15][CH3:16]参加物
5
実験手順
To a stirred solution of 20.0 g (0.14 mole) of 2-chloro-4-fluorophenol and 6.64 g (0.17 mole) of sodium hydroxide in 100 mL of water at 15° C. was added 17.7 g (0.19 mole) of methyl chloroformate. After complete addition, the mixture was stirred for 15 minutes then extracted with ethyl acetate. The organic phase was washed with a 1N sodium hydroxide solution, then dried over anhydrous magnesium sulfate. The dried extract was filtered, and the filtrate evaporated under reduced pressure to provide methyl (2-chloro-4-fluorophenyl) carbonate as a solid.
後処理
- additionAfter complete addition
- extractionthen extracted with ethyl acetate
- washThe organic phase was washed with a 1N sodium hydroxide solution
- dry with materialdried over anhydrous magnesium sulfate
- extractionThe dried extract
- filtrationwas filtered
- customthe filtrate evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-1259ba50f82d47d99279d69f323d0770
- 出典データセット
- uspto-grants-1990_03
- 特許番号
- US04906286
反応ノート
読み込み中…