Benzoyl Peroxide → 2-(Bromomethyl)-1-nitro-3-(trifluoromethyl)benzene

HRID 846028ノート

反応式

HRID 846028 の反応式
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[C:4]=1[CH3:12].[Br:15]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[F:1][C:2]([F:13])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[C:4]=1[CH2:12][Br:15]

参加物

5

反応物 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 81171alpha,alpha,alpha-Trifluoro-3-nitro-o-xylene

生成物 1

HCID 106781242-(Bromomethyl)-1-nitro-3-(trifluoromethyl)benzene収率 88.9%

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒

実験手順

A 500 mL round bottomed flask was charged with 250 mL of carbon tetrachloride 15.90 g. of 2-(trifluoromethyl)-6-nitrotoluene, 27.60 g. of N-bromosuccinimide, and 11.8 g of benzoyl peroxide. This mixture was brought under reflux and stirred at this temperature for 14 h. The mixture was cooled, filtered and 9.94 g of N-bromosuccinimide together with 4.2 g of benzoyl peroxide was added to the filtrate. This mixture was brought under reflux for 14 h. The mixture was cooled, filtered and the filtrate was stripped of solvent. The crude product was chromatographed on a SiO2 column to give 19.57 g (88.9% yield) of pure product.

後処理

  1. temperatureunder reflux
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. addition9.94 g of N-bromosuccinimide together with 4.2 g of benzoyl peroxide was added to the filtrate
  5. temperatureunder reflux for 14 h
  6. temperatureThe mixture was cooled
  7. filtrationfiltered
  8. customThe crude product was chromatographed on a SiO2 column

出典と根拠

ORDレコード
ord-c77c48c2d6b54fac95e5a0044310efba
出典データセット
uspto-grants-1992_08
特許番号
US05135838

反応ノート

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