反応 #76771
ord-3957061fae814674a25c6e9028b15568
反応方程式
溶媒
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1workup.ADDITIONwas added
- 2その他After completion of the reaction
- 3洗浄washed with chloroform
- 4抽出extracted with ethyl acetate
- 5乾燥The ethyl acetate layer was dried
- 6濃縮concentrated
実験手順
Then, 125 g (0.43 mol) of methyl 2-bromo-4-fluoro-5-nitrophenoxyformate was suspended in 200 ml of water, to which 19 g (0.47 mol) of sodium hydroxide was added, and the mixture was stirred at 50° to 60° C. for 4 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and washed with chloroform. The aqueous layer was acidified with aqueous hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was dried and concentrated, which afforded 104 g (0.43 mol) of 2-bromo-4-fluoro-5-nitrophenol.