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Iodobenzene → 2,2'-Bis(diphenylamino)-9,9'-spirobifluorene

HRID 2236963
ノート
印刷プレビュー

反応式

HRID 2236963 の反応式
[NH2:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]3([C:26]4[CH:25]=[C:24]([NH2:27])[CH:23]=[CH:22][C:21]=4[C:20]4[C:15]3=[CH:16][CH:17]=[CH:18][CH:19]=4)[C:4]=2[CH:3]=1.I[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.C[C:36]([CH3:39])([O-])[CH3:37].[Na+].C(P([C:50]([CH3:53])([CH3:52])C)C(C)(C)C)(C)(C)C>CC([O-])=O.CC([O-])=O.[Pd+2].C1(C)C=CC=CC=1>[C:29]1([N:1]([C:37]2[CH:36]=[CH:39][CH:52]=[CH:50][CH:53]=2)[C:2]2[CH:14]=[CH:13][C:12]3[C:11]4[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=4)[C:5]4([C:26]5[CH:25]=[C:24]([N:27]([C:6]6[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=6)[C:2]6[CH:14]=[CH:13][CH:12]=[CH:4][CH:3]=6)[CH:23]=[CH:22][C:21]=5[C:20]5[C:15]4=[CH:16][CH:17]=[CH:18][CH:19]=5)[C:4]=3[CH:3]=2)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 11575IodobenzeneHCID 83681Tris(1,1-dimethylethyl)phosphineHCID 154158669,9'-Spirobi[fluorene]-2,2'-diamineHCID 23676156Sodium t-butoxide

生成物 1

HCID 207338852,2'-Bis(diphenylamino)-9,9'-spirobifluorene

試薬・触媒・溶媒 2

HCID 167845
palladium(II) acetate
触媒
HCID 1140Toluene溶媒

実験手順

2,2′-diamino-9,9′-spirobifluorene (3.46 g, 10 mmol), iodobenzene (6.8 mL, 60 mmol), Pd(OAc)2 (0.112 g, 0.5 mmol), sodium-tert-butoxide (14.4 g, 150 mmol) and tri-tert-butylphosphine (20 mL, 0.05 M in toluene, 1.0 mmol) were mixed in a flask containing with toluene (100 mL). The mixture was refluxed overnight. The solution was quenched with water and extracted twice with chloroform. The combined organic extracts were dried over MgSO4 and concentrated by rotary evaporation. Column chromatography on silica gel (hexane/chloroform=4/1) afforded products [2,2′-Bis(diphenylamino)-9,9′-spirobifluorene, hereinafter named as 22DPSF] as a white solid (4.5 g, 70%).

後処理

  1. temperatureThe mixture was refluxed overnight
  2. customThe solution was quenched with water
  3. extractionextracted twice with chloroform
  4. dry with materialThe combined organic extracts were dried over MgSO4
  5. concentrationconcentrated by rotary evaporation

出典と根拠

ORDレコード
ord-3e81e2c92edb4ea69c3c5b1fa0ea0688
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07714145B2

反応ノート

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