Bromine → 2-Bromo-1-(4-cyclohexylphenyl)ethanone
反応式
[CH:1]1([C:7]2[CH:12]=[CH:11][C:10]([C:13](=[O:15])[CH3:14])=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:16]Br>C(Cl)(Cl)Cl>[Br:16][CH2:14][C:13]([C:10]1[CH:9]=[CH:8][C:7]([CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)=[CH:12][CH:11]=1)=[O:15]参加物
4
反応条件
- 温度
- 0 °C
実験手順
50 Parts of 4′-cyclohexylacetophenone was dissolved in 250 parts of chloroform, After cooled to 0° C., 40 parts of bromine was added dropwise thereto. After the reaction, the mixture was washed with 5% aqueous NaHSO3 solution, with 2% aqueous K2CO3 solution and with water, organic layer obtained was concentrated to obtain 60 parts of 2-bromo-4′-cyclohexylacetophenone.
後処理
- customAfter the reaction
- washthe mixture was washed with 5% aqueous NaHSO3 solution, with 2% aqueous K2CO3 solution and with water, organic layer
- customobtained
- concentrationwas concentrated
出典と根拠
- ORDレコード
- ord-2abd4d1de82b44f190ab96a2afe2a1d2
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07531686B2
反応ノート
読み込み中…