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Chemical Structure| 14333-93-8 Chemical Structure| 14333-93-8

Structure of 14333-93-8

Chemical Structure| 14333-93-8

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Product Details of [ 14333-93-8 ]

CAS No. :14333-93-8
Formula : C11H12O2
M.W : 176.21
SMILES Code : O=CC(C1=CC=C(CCC)C=C1)=O

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Application In Synthesis of [ 14333-93-8 ]

* 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 [ 14333-93-8 ]

[ 14333-93-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2932-65-2 ]
  • [ 14333-93-8 ]
YieldReaction ConditionsOperation in experiment
80% To a solution of SeO2 (2.70 g, 0.02 mol), 1,4-dioxane (20 mL) and H2O (1 mL) (v:v=20:1),<strong>[2932-65-2]1-(4-propylphenyl)ethanone</strong> (2.00 g, 0.01 mol) was added, and the mixture was refluxedunder nitrogen for 9 h. The solid residue was removed by filtration. The solvent was removedunder reduced pressure. Water (20 mL) was added and the resulting mixture was heated toreflux for 5 h. Upon cooling to room temperature, the solution was extracted with ethylacetate and dried over Na2SO4 The organic layer was evaporated to dryness. The cruderesidue was isolated using silica gel chromatography and was eluted with PE/EtOAc (v:v=5:1)to give 2-oxo-2-(4-propylphenyl)acetaldehyde in a yield of 80%. Then 4-aminobenzoic acid(0.50 g, 3.65 mmol) was added to a solution of 2-oxo-2-(4-propylphenyl)acetaldehyde (0.64 g,3.65 mmol) in EtOH (20 mL), and the solution was stirred at room temperature overnight.The precipitated solid was obtained by filtration and purified by recrystallization from EtOHto give 6j as white solid in a yield of 13.6%.
With selenium(IV) oxide; In 1,4-dioxane; water; for 9h;Reflux; Inert atmosphere; Add selenium dioxide (2.7g, 0.02mol), 1-(4-propylphenyl) ethanone (2g, 0.01mol) to 1,4-dioxane (20mL) and water (1mL) ( v: v = 20: 1), reflux for 9 hours under nitrogen protection.After the reaction, cool to room temperature, remove the solid residue by filtration, spin-dry the solvent under reduced pressure, add 20mL of distilled water, and reflux under nitrogen for 5h. After the reaction, cool to room temperature, It was extracted three times with ethyl acetate, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. and purify the residue by silica gel column chromatography, petroleum ether: acetone (v: v = 5: 1) to obtain the crude product 2-oxo-2- (4-propylphenyl) acetaldehyde (13-1), yield 80%.The obtained 2-oxo-2- (4-propylphenyl) acetaldehyde (0.64g, 3.65mmol), 4-aminobenzoic acid (0.5g, 3.65mmol) was added to 20mL ethanol solution at room temperature overnight The reaction was filtered and the filter cake was recrystallized from ethanol to obtain a white solid with a yield of 13.6%.
 

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