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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 849362Erstellt: 24. Oktober 2026

4-Bromodiphenyl Ether → 1-(4-Phenoxyphenyl)propan-2-one

https://huagongshe.com/de/reaction/849362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromodiphenyl EtherHCID 7565—
EduktIsopropenyl acetateHCID 7916—
EduktPotassium FluorideHCID 522689—
EduktMethoxytri-n-butylstannaneHCID 11964040—
LösungsmittelTolueneHCID 1140—
Produkt1-(4-Phenoxyphenyl)propan-2-oneHCID 1959152383%

Reaktionsschritte

75.0 g of 4-bromodiphenyl ether, 129 ml of tributyltin methoxide, 45.0 g of isopropenyl acetate and 2,47 g of dichlorobis{tri(o-tolyl)phosphine}palladium, were dissolved in 300 ml of toluene and refluxed under heating for 3 hours. The reaction solution was left to cool to room temperature, and then, a saturated potassium fluoride aqueous solution was added, followed by stirring for one hour. Then, the product was subjected to celite filtration and washed with ethyl acetate. The filtrate and washing liquid were put together. Then, the organic layer was separated and washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The drying agent was filtered off, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=15/1→10/1) to obtain 56.3 g (yield: 83%) of the above identified compound as yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06011174
Quelldatensatzuspto-grants-2000_01
ORD IDord-16f48f99f052458ab881bcbd42a77a81
Quellennotizuspto-grants-2000_01