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(2E)-1-(4-methoxyphenyl)-3-(4-methylphenyl)prop-2-en-1-one synthesis

5synthesis methods
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Yield:41564-65-2 99%

Reaction Conditions:

with sodium hydroxide in ethanol at 20; for 48 h;

Steps:

General procedure for chalcone synthesis (151-173).

General procedure: To a dry100 mL round-bottomed flask, semisynthetic acetophenone B or commercialacetophenone C or D (250 mg, between 1.22 and 2.08 mmol)and corresponding benzaldehyde (1.2 equiv.) were added, and thensolubilized in ethanol (5 mL). A NaOH 20% m/v solution (in 10 mL ofethanol) was added, and the mixture was stirred for 48 h. To stop the reaction, 5% HCl solution was added until pH ~ 7, and the mixture wasextracted with EtOAc (3x30 mL). The organic layer was dried withNa2SO4, filtered, and separated by column chromatography using ahexane/EtOAc, obtaining compounds 151-173 in yields between 27and 99%.

References:

Mellado, Marco;González, César;Mella, Jaime;Aguilar, Luis F.;Vi?a, Dolores;Uriarte, Eugenio;Cuellar, Mauricio;Matos, Maria J. [Bioorganic Chemistry,2021,vol. 108]