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Chemical Structure| 171092-38-9 Chemical Structure| 171092-38-9

Structure of 171092-38-9

Chemical Structure| 171092-38-9

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Product Details of [ 171092-38-9 ]

CAS No. :171092-38-9
Formula : C13H11NO
M.W : 197.23
SMILES Code : CC(C1=CC=CC(C2=CC=CN=C2)=C1)=O
MDL No. :MFCD12779942

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Application In Synthesis of [ 171092-38-9 ]

* 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 [ 171092-38-9 ]

[ 171092-38-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 626-60-8 ]
  • 3-acetylphenylboronic acid [ No CAS ]
  • [ 224311-51-7 ]
  • [ 171092-38-9 ]
YieldReaction ConditionsOperation in experiment
181 mg (92%) With potassium fluoride;palladium diacetate; In tetrahydrofuran; EXAMPLE 43 Synthesis of 3-(3-acetylphenyl)pyridine 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), 3-acetylphenylboronic acid (246 mg, 1.5 mmol), and potassium fluoride (173 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 3-chloropyridine (0.095 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was heated to 50° C. with stirring until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL) and poured into a separatory funnel. The mixture was washed with water (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 181 mg (92percent) of the title compound.
181 mg (92%) With potassium fluoride;palladium diacetate; In tetrahydrofuran; Example 43 Synthesis of 3-(3-acetylphenyl)pyridine 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), 3-acetylphenylboronic acid (246 mg, 1.5 mmol), and potassium fluoride (173 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 3-chloropyridine (0.095 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was heated to 50° C. with stirring until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL) and poured into a separatory funnel. The mixture was washed with water (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 181 mg (92percent) of the title compound.
 

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