Benzoyl Peroxide → 3-(Bromomethyl)-2-chloro-1,1'-biphenyl

HRID 485558ノート

反応式

HRID 485558 の反応式
[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

6

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

  1. temperatureheated
  2. temperatureto reflux with a 250 watt brooder lamp
  3. temperaturethe reaction mixture refluxed for ten minutes
  4. customThe stirred reaction mixture
  5. customwas irradiated for 16 hours
  6. temperaturecooled
  7. filtrationfiltered
  8. washThe filter cake was rinsed with carbon tetrachloride
  9. washthe combined filtrates washed with aqueous saturated sodium chloride solution
  10. dry with materialThe organic phase was dried over anhydrous magnesium sulfate
  11. filtrationfiltered
  12. customThe filtrate was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-1124f167b3bf43feb855498c40fd1a1a
出典データセット
uspto-grants-1985_08
特許番号
US04536591

反応ノート

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