Benzoyl Peroxide → 3-(Bromomethyl)-2-chloro-1,1'-biphenyl
反応式
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.[Br:33]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[Br:33][CH2:8][C:7]1[C:2]([Cl:1])=[C:3]([C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:4]=[CH:5][CH:6]=1参加物
実験手順
A stirred solution of 2-chloro-3-methyl-[1,1'-biphenyl] (0.5 g, 0.0023 mole) in 8 ml of carbon tetrachloride was irradiated and heated to reflux with a 250 watt brooder lamp. A small amount of benzoyl peroxide was added and the reaction mixture refluxed for ten minutes. A second portion of benzoyl peroxide (total 0.01 g) was added, followed by N-bromosuccinimide (0.43 g, 0.0024 mole). The stirred reaction mixture was irradiated for 16 hours, then cooled, and then filtered. The filter cake was rinsed with carbon tetrachloride and the combined filtrates washed with aqueous saturated sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to give 3-bromomethyl-2-chloro-[1,1'-biphenyl] (0.6 g) as an oil.
後処理
- temperatureheated
- temperatureto reflux with a 250 watt brooder lamp
- temperaturethe reaction mixture refluxed for ten minutes
- customThe stirred reaction mixture
- customwas irradiated for 16 hours
- temperaturecooled
- filtrationfiltered
- washThe filter cake was rinsed with carbon tetrachloride
- washthe combined filtrates washed with aqueous saturated sodium chloride solution
- dry with materialThe organic phase was dried over anhydrous magnesium sulfate
- filtrationfiltered
- customThe filtrate was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-ec0c588987724064a319fd8c5d66eeec
- 出典データセット
- uspto-grants-1983_09
- 特許番号
- US04402973
反応ノート
読み込み中…