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

3synthesis methods
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Yield:1047680-88-5 71%

Reaction Conditions:

with dipotassium peroxodisulfate;silver carbonate in acetonitrile at 100; for 24 h;Schlenk technique;Inert atmosphere;Glovebox;

Steps:

General procedure for the decarboxylative cross-coupling of α-keto acids with alkenes

General procedure: 2-oxo-2-phenylacetic acid (1a, 0.2 mmol, 30.0 mg), K2S2O8 (0.6 mmol, 162.2 mg), Ag2CO3 (5.5 mg, 0.02 mmol) were added to the Schlenk tube equipped with a magnetic stir bar in an argon-filled glove box. 1-methyl-4-vinylbenzene (2a, 1.0 mmol, 104.2 mg), MeCN (1.0 mL) were injected into the reaction tube. The reaction was then heated up to 100 °C and stirred for 24 h. Upon completion, the reaction was quenched with water and extracted with ethyl ether (3 × 10 mL). The organic layers were then combined. The pure product 3a was obtained by flash column chromatography on silica gel (petroleum/ethyl acetate= 200:1).

References:

Wu, Shang;Yu, Hongheng;Hu, Qinzheng;Yang, Quanlu;Xu, Shouwang;Liu, Tian [Tetrahedron Letters,2017,vol. 58,# 51,p. 4763 - 4765] Location in patent:supporting information