Cesium carbonate → 2-Cyclohexyl-4-(4-hexylphenylethynyl)-1-(4-propylphenylethynyl)benzene

HRID 931856노트

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HRID 931856 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][C:10]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=2)=[C:4]([CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)[CH:3]=1.C(C1C=CC(C#C)=CC=1)CC.C(=O)([O-])[O-].[Cs+].[Cs+].C1(P(C2CCCCC2)[C:47]2[CH:52]=[CH:51][CH:50]=[CH:49][C:48]=2[C:53]2[C:58](C(C)C)=[CH:57][C:56]([CH:62](C)[CH3:63])=[CH:55][C:54]=2C(C)C)CCCCC1.O1[CH2:79][CH2:78]OCC1>CC#N.CC#N.Cl[Pd]Cl.O>[CH:17]1([C:4]2[CH:3]=[C:2]([C:63]#[C:62][C:56]3[CH:57]=[CH:58][C:53]([CH2:48][CH2:47][CH2:52][CH2:51][CH2:50][CH3:49])=[CH:54][CH:55]=3)[CH:7]=[CH:6][C:5]=2[C:8]#[C:9][C:10]2[CH:11]=[CH:12][C:13]([CH2:16][CH2:78][CH3:79])=[CH:14][CH:15]=2)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1

참가 물질

8

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온도
100 °C

실험 절차

4.5 g (11.87 mmol) of 10, 1.7 g (11.87 mmol) of 1-n-propyl-4-ethynylbenzene, 8.5 g (26.12 mmol) of caesium carbonate, 30 mg (0.1 mmol) of bis(acetonitrile)palladium(II) chloride and 170 mg (0.35 mmol) of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl are dissolved in 35 ml of dioxane under nitrogen and heated at 100° C. overnight. 100 ml of water are added to the cooled solution, and the mixture is extracted twice with methyl t-butyl ether (100 ml). The combined organic phases are washed with water, dried over sodium sulfate and evaporated in vacuo. The residue is purified by column chromatography, giving the title compound 6 as a solid.

후처리

  1. extractionthe mixture is extracted twice with methyl t-butyl ether (100 ml)
  2. washThe combined organic phases are washed with water
  3. dry with materialdried over sodium sulfate
  4. customevaporated in vacuo
  5. customThe residue is purified by column chromatography

출처 및 근거

ORD 기록
ord-4680b74a671641f881642c3355dfb9c5
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09296948B2

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