Bromine → 2-Bromo-1-(4-iodophenyl)ethanone
反応式
[I:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.[Br:11]Br>O1CCOCC1>[Br:11][CH2:9][C:8]([C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1)=[O:10]参加物
4
実験手順
A solution of 1-(4-iodophenyl)ethanone (55.9 mmol) in dioxane (160 mL) was cooled to 10° C. Bromine (1.1 equiv, 61.6 mmol) was added dropwise to the reaction mixture. After 10 min, the cooling bath was removed and the reaction mixture was stirred at room temperature. After 1.5 h, the reaction mixture was concentrated in vacuo, poured into water (100 mL), and extracted with (3×100 mL) ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to a tan solid (18.2 g) which was used directly in the next step.
後処理
- customthe cooling bath was removed
- waitAfter 1.5 h
- concentrationthe reaction mixture was concentrated in vacuo
- additionpoured into water (100 mL)
- extractionextracted with (3×100 mL) ethyl acetate
- dry with materialThe combined organic layers were dried over sodium sulfate
- concentrationconcentrated in vacuo to a tan solid (18.2 g) which
出典と根拠
- ORDレコード
- ord-b0308772db1a4e8f9007e79ae1fd101b
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07582668B2
反応ノート
読み込み中…