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Chemical Structure| 114772-33-7 Chemical Structure| 114772-33-7

Structure of 114772-33-7

Chemical Structure| 114772-33-7

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Product Details of [ 114772-33-7 ]

CAS No. :114772-33-7
Formula : C15H14O2
M.W : 226.27
SMILES Code : O=C(C1=CC(C2=CC=C(C)C=C2)=CC=C1)OC
MDL No. :MFCD05981251

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Application In Synthesis of [ 114772-33-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 114772-33-7 ]

[ 114772-33-7 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 2905-65-9 ]
  • [ 5720-05-8 ]
  • [ 114772-33-7 ]
  • 3
  • [ 67-56-1 ]
  • [ 147404-69-1 ]
  • [ 114772-33-7 ]
YieldReaction ConditionsOperation in experiment
77% With sulfuric acid; for 5h;Reflux; General procedure: 4‘-Methyl-[1,1‘-biphenyl]-carboxylicacid (0.25 g, 1.18 mmol) was suspended with stirring in10 ml of abs. methanol. Subsequently, 0.13 ml of conc. H2SO4were added and the mixture was heated to reflux for 5h. After cooling to RT, 10ml of water were added and the product was extracted with methylene chloride.The combined organic layers dried over sodium sulfate and the solvent wasevaporated in vacuo. The crude product was purified by column chromatography onsilica gel with methylene chloride/methanol (95:5).
  • 4
  • [ 2905-65-9 ]
  • [ 380481-66-3 ]
  • [ 114772-33-7 ]
YieldReaction ConditionsOperation in experiment
97% With potassium phosphate tribasic hydrate; NiIICl(1-naphthyl)(tricyclohexylphosphine)2; tricyclohexylphosphine; In tetrahydrofuran; at 23℃; for 4h;Inert atmosphere; Glovebox; Sealed tube; General procedure: Cross-Coupling of ortho-, meta-, and para-Substituted, Electron-Rich and Electron-Deficient Aryl Halides and Aryl Mesylates with Aryl Neopentylglycolboronates Catalyzed by NiIICl(1-naph-thyl)(PCy3)2/PCy3 in Anhydrous THF at 23 C; General Procedure 2In an oven-dried test tube charged with a Teflon coated stirring barwere added aryl halide or aryl mesylate (0.3 mmol), aryl neopentyl-glycolboronates (0.315 mmol), K3PO4(H2O)3.2 (191.00 ± 1.00 mg, 0.9mmol), and NiIICl(1-naphthyl)(PCy3)2 (11.73 ± 0.0510 mg, 0.015mmol, 5% catalyst loading). The test tube was brought into a N2 filledglove box (moisture level <2 ppm) through three degassing cycles andPCy3 (8.4 mg, 0.03 mmol, 10% loading) ligand was added. Distilled sol-vent (1 mL) was added inside the glove box and the test tube wassealed by a rubber septum and left stirring at 23 C. A sample was tak-en by syringe and transferred outside the glove box. The sample wasdiluted by distilled THF (0.2 mL) and filtered through a short columnof Al2O3. The filtrate was concentrated and the GC analysis was car-ried out. The reaction mixture was diluted with CH2Cl2 (2 mL), filteredthrough a layer of Al2O3, and washed with CH2Cl2 (3 1 mL). The fil-trate was collected and concentrated under vacuum. The crude prod-uct was purified by column chromatography on silica gel with EtO-Ac/hexane mixture as eluent. The reductive elimination side-productwas also isolated and characterized.
 

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