Ethylenediamine → 4-Cyano-2'-nitrodiphenyl

HRID 258059ノート

反応式

HRID 258059 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]1[CH:15]=[CH:14][C:13](Br)=[CH:12][CH:11]=1)([O-:3])=[O:2].[Cu](C#N)[C:18]#[N:19].CN(C=O)C.C(N)CN>O.CC(C)=O>[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]1[CH:15]=[CH:14][C:13]([C:18]#[N:19])=[CH:12][CH:11]=1)([O-:3])=[O:2]

参加物

7

反応物 4

HCID 3301EthylenediamineHCID 6228DimethylformamideHCID 218576474'-Bromo-2-nitrobiphenylHCID 178418260HCID 178418260、化合物

生成物 1

HCID 118511144-Cyano-2'-nitrodiphenyl

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 962Water溶媒

実験手順

20 g (7.19 10-2 moles) of 4 nitro 4'bromobiphenyl, 11.6 of copper cyanide and 120 ml of DMF are placed in a 250 ml receptacle with a magnetic agitator. The mixture is refluxed for 5 h 30. It is then allowed to cool, acetone is added and the reaction medium is poured into 2 liters of water containing 2 g of ethylene diamine. A precipitate is formed. The solid is filtered out then washed in water and hexane. This raw product is redissolved in chloroform. The organic phase is dried on MgSO4, filtered and evaporated till dry. The solid obtained is recrystallized in an ethanol-chloroform mixture. This provides 13.16 g of product, yield ρ=81.7%, melting point=195° C.

後処理

  1. temperatureThe mixture is refluxed for 5 h 30
  2. temperatureto cool
  3. customA precipitate is formed
  4. filtrationThe solid is filtered
  5. washout then washed in water
  6. dissolutionThis raw product is redissolved in chloroform
  7. customThe organic phase is dried on MgSO4
  8. filtrationfiltered
  9. customevaporated
  10. customtill dry
  11. customThe solid obtained
  12. customis recrystallized in an ethanol-chloroform mixture

出典と根拠

ORDレコード
ord-1ad01d141bc0437d83f2cc676e142a63
出典データセット
uspto-grants-1993_11
特許番号
US05264512

反応ノート

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