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Water → 1,3-Bis(3,6-di-tert-butylcarbazol-9-yl)benzene

HRID 1037506
ノート
印刷プレビュー

反応式

HRID 1037506 の反応式
[CH:1]1[C:13]2[N:12]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([N:20]4[C:32]5[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=5[C:26]5[C:21]4=[CH:22][CH:23]=[CH:24][CH:25]=5)[CH:15]=3)[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[Cl-].[Cl-].[Cl-].[Al+3].O.Cl[C:39]([CH3:42])([CH3:41])[CH3:40]>>[C:39]([C:8]1[CH:9]=[CH:10][C:11]2[N:12]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([N:20]4[C:21]5[CH:22]=[CH:23][C:24]([C:5]([CH3:6])([CH3:13])[CH3:4])=[CH:25][C:26]=5[C:27]5[C:32]4=[CH:31][CH:30]=[C:29]([C:26]([CH3:27])([CH3:21])[CH3:25])[CH:28]=5)[CH:15]=3)[C:13]3[C:5]([C:6]=2[CH:7]=1)=[CH:4][C:3]([C:39]([CH3:42])([CH3:41])[CH3:40])=[CH:2][CH:1]=3)([CH3:42])([CH3:41])[CH3:40]
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 4

HCID 962WaterHCID 10486tert-BUTYL CHLORIDEHCID 6451240Aluminum(III) Chloride2 回HCID 220203771,3-Bis(N-carbazolyl)benzene2 回

生成物 1

HCID 597755151,3-Bis(3,6-di-tert-butylcarbazol-9-yl)benzene

実験手順

To a solution of 1,3-di(carbazol-9-yl)benzene (1.0 g, 2.45 mmol) in 2-chloro-2-methylpropane (10.0 ml) was added aluminum trichloride (0.32 g, 2.40 mmol) at room temperature under nitrogen atmosphere and stirring. After the addition of AlCl3, insoluble 1,3-di(carbazol-9-yl)benzene disappeared within minutes. The green solid appeared after 5 minutes of reacting at room temperature. The reaction was carried out at room temperature for another 10 minutes. TLC showed that the reaction was finished. After which, water (20.0 ml) was added and the green solid became white. The solid product was collected with filtration and washed with methanol. The product was purified by recrystallization from acetone/THF/methanol to yield a white solid in the amount of 1.23 g (79.4%).

後処理

  1. waitdisappeared within minutes
  2. customof reacting at room temperature
  3. waitThe reaction was carried out at room temperature for another 10 minutes
  4. filtrationThe solid product was collected with filtration
  5. washwashed with methanol
  6. customThe product was purified by recrystallization from acetone/THF/methanol
  7. customto yield a white solid in the amount of 1.23 g (79.4%)

出典と根拠

ORDレコード
ord-4df7734bacbf40279c98f0f3180ba066
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08546505B2

反応ノート

読み込み中…

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