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Chemical Structure| 7372-85-2 Chemical Structure| 7372-85-2

Structure of 7372-85-2

Chemical Structure| 7372-85-2

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Product Details of [ 7372-85-2 ]

CAS No. :7372-85-2
Formula : C14H14
M.W : 182.26
SMILES Code : CC1=CC=C(C)C(C2=CC=CC=C2)=C1

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Application In Synthesis of [ 7372-85-2 ]

* 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 [ 7372-85-2 ]

[ 7372-85-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 553-94-6 ]
  • [ 224311-51-7 ]
  • [ 98-80-6 ]
  • [ 7372-85-2 ]
YieldReaction ConditionsOperation in experiment
149 mg (82%) With potassium fluoride;palladium diacetate; In tetrahydrofuran; EXAMPLE 36 Synthesis of 2,5-dimethylbiphenyl An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol percent), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol percent), phenylboronic acid (183 mg. 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-bromo-p-xylene (0.138 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 149 mg (82percent) of the title compound.
149 mg (82%) With potassium fluoride;palladium diacetate; In tetrahydrofuran; Example 36 Synthesis of 2,5-dimethylbiphenyl An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol percent), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol percent), phenylboronic acid (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-bromo-p-xylene (0.138 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 149 mg (82percent) of the title compound.
 

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