Toluene → N,N'-diphenyl-N,N'-bis[3-(2-ethoxycarbonylethyl)phenyl]-[1,1'-biphenyl]-4,4'-diamine

HRID 1451662ノート

反応式

HRID 1451662 の反応式
[C:1]1([NH:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]3[CH:26]=[CH:25][C:17]([NH:18][C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)=[CH:16][CH:15]=3)=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.I[C:28]1[CH:29]=[C:30]([CH:38]=[CH:39][CH:40]=1)[CH2:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34].[C:41](=[O:44])([O-])[O-:42].[K+].[K+].CCCCC[CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH3:59].[C:60]1(C)C=CC=C[CH:61]=1>O.O.O.O.O.S([O-])([O-])(=O)=O.[Cu+2]>[C:19]1([N:18]([C:58]2[CH:57]=[CH:56][CH:55]=[C:54]([CH2:53][CH2:52][C:41]([O:42][CH2:60][CH3:61])=[O:44])[CH:59]=2)[C:17]2[CH:25]=[CH:26][C:14]([C:11]3[CH:12]=[CH:13][C:8]([N:7]([C:1]4[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=4)[C:28]4[CH:40]=[CH:39][CH:38]=[C:30]([CH2:31][CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH:29]=4)=[CH:9][CH:10]=3)=[CH:15][CH:16]=2)[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1

参加物

7

反応物 5

HCID 1140TolueneHCID 11430Potassium CarbonateHCID 12388TridecaneHCID 68280N,N'-DiphenylbenzidineHCID 10913723Ethyl 3-iododihydrocinnamate

生成物 1

HCID 11125317N,N'-diphenyl-N,N'-bis[3-(2-ethoxycarbonylethyl)phenyl]-[1,1'-biphenyl]-4,4'-diamine

試薬・触媒・溶媒 1

HCID 24463Copper sulfate pentahydrate触媒

反応条件

温度
230 °C

実験手順

Into a 100-ml flask were introduced 10.77 g of N,N'-diphenylbenzidine, 23.0 g of ethyl 3-iododihydrocinnamate, 11.61 g of potassium carbonate, 1.0 g of copper sulfate pentahydrate, and 20 ml of n-tridecane. The reactants were reacted with heating at 230° C. for 1 hour under an atmosphere of nitrogen. After the reaction, the reaction mixture was cooled to room temperature and then dissolved into 50 ml of toluene. Insolubles were filtered off, and the filtrate was purified by silica gel column chromatography using toluene. As a result, 19.6 g of N,N'-diphenyl-N,N'-bis[3-(2-ethoxycarbonylethyl)phenyl]-[1,1'-biphenyl]-4,4'-diamine was obtained as an oily substance. An IR spectrum of this compound is shown in FIG. 1.

後処理

  1. customThe reactants were reacted
  2. customAfter the reaction
  3. temperaturethe reaction mixture was cooled to room temperature
  4. filtrationInsolubles were filtered off
  5. customthe filtrate was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-a3077e2c2d60465cb0fac151563a52de
出典データセット
uspto-grants-1997_02
特許番号
US05604064

反応ノート

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