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[ CAS No. 944902-15-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 944902-15-2
Chemical Structure| 944902-15-2
Structure of 944902-15-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 944902-15-2 ]

CAS No. :944902-15-2 MDL No. :MFCD18074122
Formula : C9H9NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 163.17 Pubchem ID :-
Synonyms :

Safety of [ 944902-15-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H320-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 944902-15-2 ]

* 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 [ 944902-15-2 ]

[ 944902-15-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 944902-15-2 ]
  • [ 74-88-4 ]
  • [ 120686-09-1 ]
YieldReaction ConditionsOperation in experiment
General procedure: The pyridone21 (1.0 equiv) was stirred with a mixture of Ag2CO3 (2.0 equiv) and iodoalkanes (5.0 equiv) in chloroform (0.2 M) in dark at room temperature overnight. The mixture was filtrated, concentrated and purified by flash chromatography to give differently-protected pyridones, which were further refluxed in 5% HCl-acetone (1:1, 0.1 M) overnight. Acetone was removed and the aqueous layer was basified with solid NaHCO3, and then extracted with ethyl acetate. The organic extracts were washed with brine, dried over anhydrous Na2SO4, and concentrated. The resulting ketone was directly used in the next step. The resulting ketone (1.0 equiv) in certain carbonate was added dropwise to a mixture of NaH (1.1 equiv) in the carbonate (0.2 M) under nitrogen at room temperature. The mixture was refluxed until disappearance of the starting material on the TLC. The reaction was quenched with saturated aq NH4Cl. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried, and concentrated. Flash chromatography on silica gel gave the beta-ketoesters 10b, 10d, 10e, and 10f.
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