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Chemical Structure| 18600-54-9 Chemical Structure| 18600-54-9

Structure of 18600-54-9

Chemical Structure| 18600-54-9

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Product Details of [ 18600-54-9 ]

CAS No. :18600-54-9
Formula : C15H11NO2
M.W : 237.25
SMILES Code : O=C1OC(C2=CC=C(C)C=C2)=NC3=CC=CC=C13
MDL No. :MFCD00024128

Safety of [ 18600-54-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 18600-54-9 ]

* 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 [ 18600-54-9 ]

[ 18600-54-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 55577-25-8 ]
  • [ 18600-54-9 ]
YieldReaction ConditionsOperation in experiment
80% General procedure: A mixture of compound 1 (0.20 mmol), CuCl (4.0 mg, 0.04 mmol) and Na2CO3(42 mg, 0.40 mmol) in DMSO (1.0 mL) was stirred at 80 C under an oxygen atmosphere (1 atm). After 12 h, Ac2O (1.0 mmol) was added,and the mixture wasstirred for an additional 0.5 h. Then, the mixture wasquenched with 10% HCl at 0 C and extracted with EtOAc. The organic extracts were washed with H2O and brine, dried over Na2SO4, andthen concentrated. The crude product was chromatographed on silica gel.
66% With [bis(acetoxy)iodo]benzene; water; In N,N-dimethyl-formamide; at 60℃; for 24h; General procedure: A mixture of 1 (1.0 mmol), PhI(OAc)2 (1.288 g, 4.0 mmol), and H2O (180 μL, 10 mmol) in DMF (10 mL) was stirred at 60 C under air for 24 h, and then the mixture was cooled to r.t. The mixture was quenched with H2O (30 mL) and extracted with EtOAc. The organic extracts were washed with brine, dried over Na2SO4, and then concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, PE-EtOAc) to give the corresponding product.
 

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