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Chemical Structure| 57120-36-2 Chemical Structure| 57120-36-2

Structure of 57120-36-2

Chemical Structure| 57120-36-2

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Product Details of [ 57120-36-2 ]

CAS No. :57120-36-2
Formula : C10H15NO
M.W : 165.23
SMILES Code : NC1=CC=C(OC(C)(C)C)C=C1
MDL No. :MFCD11196184
InChI Key :NJLJXOXRYXXBOF-UHFFFAOYSA-N
Pubchem ID :11159518

Safety of [ 57120-36-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317
Precautionary Statements:P280

Application In Synthesis of [ 57120-36-2 ]

* 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 [ 57120-36-2 ]

[ 57120-36-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 18995-35-2 ]
  • [ 57120-36-2 ]
YieldReaction ConditionsOperation in experiment
75% With ammonium hydroxide; potassium phosphate; copper(l) iodide; N-(biphenyl-2-one)-1H-indole-2-carboxamide; In dimethyl sulfoxide; at 110℃; for 24h;Schlenk technique; Inert atmosphere;Catalytic behavior; General procedure: Copper iodide (0.05 mmol), ligand L-15 (0.05 or 0.1 mmol), potassium phosphate (1.1 mmol) were added into a 10 mL Schlenk tube. The tube was then evacuated and filled with argon for three times, and then aryl chloride (1.0 mmol), 1 mL of DMSO and ammonium hydroxide (2.0 mmol) were added. The reaction mixture was homogeneously stirred at 110 C. or 120 C. for 24 hours. After cooling, water and ethyl acetate were added and separated. The aqueous phase was extracted twice with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate. After concentration, the residue was purified by column chromatography to give the product aromatic amines.
73% With ammonium hydroxide; potassium phosphate; copper(l) iodide; N1,N2-bis(5-methyl-[1,1'-biphenyl]-2-yl)oxalamide; In dimethyl sulfoxide; at 110℃; for 24h;Inert atmosphere; Schlenk technique; Example 9 Synthesis of Aromatic Amines Copper iodide (0.05 mmol), ligand L-II-71 (0.05 or 0.1 mmol), potassium phosphate (1.1 mmol) were added into a 10 mL of Schlenk tube. The tube was then evacuated and backfilled with argon (this sequence was repeated three times), and then aryl chloride (1.0 mmol), 1 mL of DMSO and ammonium hydroxide (2.0 mmol) were added. The reaction mixture was well stirred at 110C. or 120C. for 24 hours. After cooling, water and ethyl acetate were added and mixture was separated. The aqueous phase was extracted twice with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate. After concentration, the residue was purified by column chromatography to give the product aromatic amines.
  • 2
  • [ 18995-35-2 ]
  • [ 57120-36-2 ]
  • C20H27NO2 [ No CAS ]
 

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