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Chemical Structure| 613-40-1 Chemical Structure| 613-40-1

Structure of 613-40-1

Chemical Structure| 613-40-1

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Product Details of [ 613-40-1 ]

CAS No. :613-40-1
Formula : C14H14O
M.W : 198.26
SMILES Code : CCOC1=CC=C(C2=CC=CC=C2)C=C1

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Application In Synthesis of [ 613-40-1 ]

* 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 [ 613-40-1 ]

[ 613-40-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 108-86-1 ]
  • [ 22237-13-4 ]
  • [ 613-40-1 ]
YieldReaction ConditionsOperation in experiment
99% With dichloro bis(acetonitrile) palladium(II); C95H120N20O10(10+)*10F6P(1-); potassium carbonate; In ethanol; at 50℃; for 1.5h; General procedure: In a typical run, a mixture of aryl bromide (0.50 mmol),phenylboronic acid (0.55 mmol), K2CO3 (1.5 mmol),0.2 mol% ligand, 1 mol% PdCl2(CH3CN)2 in 1.5 mL of ethanol were stirred at 50 C for 1.5 h under air. Solvent ethanol was removed completely under vacuum degree0.09 MPa at 45 C to give a crude product. The pure product was isolated by column chromatography on silica.
93% With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; cesium fluoride; In 1,2-dimethoxyethane; at 80℃; for 6.5h;Schlenk technique; Inert atmosphere; General procedure: A Schlenk tube was dried under vacuum, filled with nitrogen and charged consecutively with 1.00 eq bromine substrate, 1.00 eq boronic acid, 2.10 eq CsF, 0.05 eq PdCl2(dppf)*DCM and anhydrous DME (2 mL/0.15 mmol bromoarene). The suspension was degassed by vacuum/N2 cycles and stirred at 80 C. As TLC analysis or GC-MS analysis indicated full conversion of the starting material, the reaction mixture was cooled to rt and filtered through a pad of celite, which was rinsed with EtOAc and/or DCM. The solvent from the filtrate was removed under reduced pressure and final purification by column chromatography or silica gel filtration yielded the pure product.
 

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