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4-Bromo-4'-iodobiphenyl → N4'-(4'-bromobiphenyl-4-yl)-N4,N4'-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4'-diamine

HRID 889802
ノート
印刷プレビュー

反応式

HRID 889802 の反応式
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N:9]([C:31]1[CH:36]=[CH:35][C:34]([CH3:37])=[CH:33][CH:32]=1)[C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([NH:22][C:23]3[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][C:24]=3[CH3:30])=[CH:18][CH:17]=2)=[CH:12][CH:11]=1.[Br:38][C:39]1[CH:44]=[CH:43][C:42]([C:45]2[CH:50]=[CH:49][C:48](I)=[CH:47][CH:46]=2)=[CH:41][CH:40]=1>[Cu].ClC1C=CC=CC=1Cl>[Br:38][C:39]1[CH:44]=[CH:43][C:42]([C:45]2[CH:50]=[CH:49][C:48]([N:22]([C:23]3[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][C:24]=3[CH3:30])[C:19]3[CH:20]=[CH:21][C:16]([C:13]4[CH:12]=[CH:11][C:10]([N:9]([C:3]5[CH:4]=[CH:5][C:6]([CH3:8])=[CH:7][C:2]=5[CH3:1])[C:31]5[CH:36]=[CH:35][C:34]([CH3:37])=[CH:33][CH:32]=5)=[CH:15][CH:14]=4)=[CH:17][CH:18]=3)=[CH:47][CH:46]=2)=[CH:41][CH:40]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 109044524-Bromo-4'-iodobiphenylHCID 86597908N4,N4'-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4'-diamine

生成物 1

HCID 69525885N4'-(4'-bromobiphenyl-4-yl)-N4,N4'-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4'-diamine

試薬・触媒・溶媒 2

HCID 23978Copper触媒HCID 72391,2-Dichlorobenzene溶媒

実験手順

Into a 2 liter three-necked reaction vessel fitted with an air-cooling tube and a mechanical stirrer, 48.3 g (0.1 mol) of N4,N4′-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4′-diamine, 39.5 g (0.11 mol) of 4′-bromo-4-iodobiphenyl, 20 g of copper powder and 200 mL of o-dichlorobenzene were introduced and heated for 12 hours in an oil bath. After the reaction was completed, the reaction mixture was left to cool to room temperature, followed by removing solid matter by filtration, and thereafter extraction with toluene/water. Then, the solvent was distilled away from the organic layer under reduced pressure, followed by purification with a silica gel column (developer solvent: hexane/toluene=2:1) to give the desired N4′-(4′-bromobiphenyl-4-yl)-N4,N4′-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4′-diamine. The compound obtained was in a yield of 45.0 g corresponding to 63%. The compound obtained was measured with the same elementary analyzer as the above.

後処理

  1. customInto a 2 liter three-necked reaction vessel fitted with an air-cooling tube and a mechanical stirrer
  2. temperatureheated for 12 hours in an oil bath
  3. waitthe reaction mixture was left
  4. customby removing solid matter
  5. filtrationby filtration
  6. extractionextraction with toluene/water
  7. distillationThen, the solvent was distilled away from the organic layer under reduced pressure
  8. customfollowed by purification with a silica gel column (developer solvent: hexane/toluene=2:1)

出典と根拠

ORDレコード
ord-0778d2c945ff4e1386f6f60b3961e346
出典データセット
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06994941B2

反応ノート

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