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2'-CHLORO-3-PHENYLPROPIOPHENONE synthesis

8synthesis methods
-

Yield:898764-45-9 89 %Spectr.

Reaction Conditions:

with chloro(η5-pentamethylcyclopentadienyl)(η2-pyridine-2-carboxylato)iridium(III);potassium hydroxide in toluene at 120; for 2 h;

Steps:

4.4 General procedure for the alpha alkylation of ketones with alcohols

General procedure: The reaction was carried out in Radleys Carousel 12 Plus Reaction Station. The substrates (ketone (1.0mmol)/alcohol (1.0mmol)), catalyst (0.002mmol), KOH (0.2mmol), and 1,3,5-trimethoxybenzene (used as an internal standard) were combined in an oven-dried Radleys tube. Toluene (1.0ml) was added to the tube, and the mixture was refluxed under air for 2h at 120°C. The reaction was cooled and diluted with EtOAc, and the reaction mixture was filtered through a pad of Celite. The filtrate was concentrated under reduced pressure, and the resulting residue was analyzed by 1H NMR.

References:

Pakyapan, Bilge;Kavukcu, Serdar Bat?kan;?ahin, Zarife Sibel;Türkmen, Hayati [Journal of Organometallic Chemistry,2020,vol. 925,art. no. 121486]