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1.3- Diphenyl-2-propen

As actually carried out the mixed aldol condensation product 1 3 diphenyl 2 propen 1 one has been isolated in 85% yield on treating benzaldehyde with ace tophenone in an aqueous ethanol solution of sodium hydroxide at 15-30°C... [Pg.775]

C15H120 trans-1,3-diphenyl-2-propen-1 -one 614-47-1 62.00 1.0712 1 28325 C15H1405 bis(2-hydroxy-4-methoxyphenyl)methanone 131-54-4 25.00 1.2549 2... [Pg.272]

The Corey-Chaykovsky reaction will be used to cyclopropanate your chalcone from Experiment 61. The reaction involves the reaction of trimethylsulfoxonium iodide and potassium fcrf-butoxide in anhydrous dimethylsulfoxide (DMSO). The reaction is stirred at room temperature for 1 hr. For example, frans-chalcone (1,3-diphenyl-2-propen-l-one) produces an 88% yield of the cyclopropanated product. You will analyze your product by NMR and infrared spectroscopy. [Pg.560]


See other pages where 1.3- Diphenyl-2-propen is mentioned: [Pg.775]    [Pg.778]    [Pg.775]    [Pg.205]    [Pg.240]    [Pg.782]    [Pg.785]    [Pg.272]    [Pg.272]    [Pg.528]    [Pg.720]    [Pg.723]    [Pg.720]    [Pg.723]    [Pg.342]    [Pg.343]    [Pg.334]    [Pg.335]    [Pg.909]    [Pg.831]    [Pg.847]    [Pg.321]    [Pg.322]    [Pg.366]    [Pg.367]    [Pg.364]    [Pg.117]    [Pg.375]    [Pg.334]    [Pg.1024]    [Pg.1115]    [Pg.1174]    [Pg.1289]    [Pg.1364]   


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1.3- Diphenyl-2-propen-1 -one

2,3-Diphenyl-1-propene

2,3-Diphenyl-1-propene

3-acetoxy-1,3-diphenyl-1 propene

Diphenyl-2-propen-l-one

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