Azobisisobutyronitrile → 1-(Bromomethyl)-2-chloro-4-nitrobenzene

HRID 572994

反応式

HRID 572994 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH3:11].[Br:12]N1C(=O)CCC1=O.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:12][CH2:11][C:3]1[CH:4]=[CH:5][C:6]([N+:8]([O-:10])=[O:9])=[CH:7][C:2]=1[Cl:1]

参加物

5

反応物 3

HCID 6547AzobisisobutyronitrileHCID 84912-Chloro-4-nitrotolueneHCID 67184N-bromobutanimide

生成物 1

HCID 30163681-(Bromomethyl)-2-chloro-4-nitrobenzene

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒

実験手順

A suspension of 2-chloro-4-nitrotoluene (10.0 g, 58.3 mmol), N-bromosuccinimide (NBS, 10.9 g, 61.2 mmol), and 2,2′-azobis(2-methylpropionitrile) (AIBN, 0.29 g, 1.75 mmol) in 120 mL of CCl4 was heated at reflux under an atmosphere of N2 for 12 h. The reaction mixture was cooled to ambient temperature, and the solid was filtered and washed with EtOAc. The combined filtrate was washed with aq. NaHCO3, dried over Na2SO4, filtered, concentrated on rotovap, and further dried under vacuum. 1H NMR indicated the ratio of desired product to unreacted 2-chloro-4-nitrotoluene to be 50:50. This material was used directly in the next step.

後処理

  1. temperaturewas heated
  2. temperatureat reflux under an atmosphere of N2 for 12 h
  3. filtrationthe solid was filtered
  4. washwashed with EtOAc
  5. washThe combined filtrate was washed with aq. NaHCO3
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated on rotovap
  9. customfurther dried under vacuum

出典と根拠

ORDレコード
ord-a303321847cc4512bca81399b8c71c56
出典データセット
uspto-grants-2015_05
特許番号
US09029533B2

関連ノート

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