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Chemical Structure| 14159-59-2 Chemical Structure| 14159-59-2

Structure of 14159-59-2

Chemical Structure| 14159-59-2

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Product Details of [ 14159-59-2 ]

CAS No. :14159-59-2
Formula : C8H11N
M.W : 121.18
SMILES Code : C(C1C=CC=NC=1C)C
English Name :Pyridine, 3-ethyl-2-methyl-
MDL No. :MFCD00137530

Safety of [ 14159-59-2 ]

Application In Synthesis of [ 14159-59-2 ]

* 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 [ 14159-59-2 ]

[ 14159-59-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 107-87-9 ]
  • [ 109-76-2 ]
  • [ 622-39-9 ]
  • [ 14159-59-2 ]
YieldReaction ConditionsOperation in experiment
With oxygen; copper diacetate; palladium diacetate In dimethyl sulfoxide at 120℃; for 15h; Overall yield = 13 %; 5,6-Dihydrobenzo[h]quinoline8 (9) General procedure: Pd(OAc)2 (9.00 mg, 0.04 mmol) and () (14.6 mg, 0.08 mmol) were placed in a screw-top test tube, and a solution of 3,4-dihydronaphthalen-l(2H)-one (8) (58.6 mg, 0.40 mmol) in DMSO (0.08 mL) was added at room temperature. Then 1,3-diaminopropane (6) (0.10 mL, 1.20 mmol) was added to the reaction mixture. The test tube was filled with oxygen and then the resulting mixture was stirred at 120 °C for 16 h. After cooling down to room temperature, the palladium residue was removed by filtering through Celite. The organic solvent was removed under reduced pressure, and then the reaction was quenched by addition of 10% aqueous NH3 solution. The solution was extracted three times with a 4:1 mixture of hexane and EtOAc. The combined organic layers were washed with saturated aqueous NaCl solution, dried over anhydrous Na2S04, and filtered through Celite. The filtrate was concentrated to afford 5,6-dihydrobenzo[h]quinoline (9) (51.1 mg, 70%) as a yellow oil.
 

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