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[ CAS No. 1380602-57-2 ] {[proInfo.proName]}

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Chemical Structure| 1380602-57-2
Chemical Structure| 1380602-57-2
Structure of 1380602-57-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1380602-57-2 ]

CAS No. :1380602-57-2 MDL No. :MFCD22574091
Formula : C15H17NO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 227.30 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1380602-57-2 ]

* 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 [ 1380602-57-2 ]

[ 1380602-57-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 529-23-7 ]
  • [ 7307-04-2 ]
  • [ 1380602-57-2 ]
YieldReaction ConditionsOperation in experiment
81% Stage #1: o-aminobenzaldehyde; acetylpinacolin With lanthanide(III)chloride heptahydrate; acetic acid at 60℃; Stage #2: With sodium hydroxide In water; ethyl acetate at 20℃; regioselective reaction; 14. A typical experimental procedure. General procedure: To a reaction vial loaded with substituted 1,3-diketone (0.24 mmol), amino benzaldehyde, (0.2 mmol) and lanthanum chloride heptahydrate was added acetic acid (3.5 mL). The resulting suspension was heated to 60 °C for 3-5 h. The reaction progress was monitored by LC-MS. At the completion, the reaction mixture was allowed to cool to room temperature. Ethyl acetate (5 mL) was added and the resulting mixture was washed with water (5 mL) and 1 N NaOH (5 mL), the organic layer was dried on MgSO4 and concentrated to give a crude product. The major quinoline product was isolated by column chromatography.
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