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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28762Erstellt: 23. Oktober 2026

Lead tetraacetate → p-Methoxyphenylpropionic acid

https://huagongshe.com/de/reaction/28762

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLead tetraacetateHCID 11025—
EduktPerchloric AcidHCID 24247—
EduktEthyl orthoformateHCID 31214—
Edukt4-PropanoylanisoleHCID 67144—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelPotassium HydroxideHCID 14797—
Produktp-Methoxyphenylpropionic acidHCID 25757663,5%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90% lead(IV)acetate (6.45 g, 14.5 mmol), triethylorthoformate (15 ml) and 70% perchloric acid (1.2 ml. 29 mmol) was heated to 55° C. for 18 h. The mixture was cooled and the triethylorthoformate removed under reduced pressure. The residue was dissolved in CHCl3 and the remaining precipitate filtered off and discarded. The CHCl3 solution was then washed with water and evaporated to yield the crude ester. This crude ester product was dissolved in a 10% KOH 1:1 water:methanol solution, which was then refluxed for 3 h. After cooling the methanol was evaporated under reduced pressure and the aqueous solution washed with diethylether (3×25 ml). The aqueous solution was acidified with 2N H2SO4, then washed again with diethylether (3×25 ml). The combined fractions from the second ether wash were dried (Na2SO4) and evaporated to give the propionic acid (1.66 g, 63%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419998B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-296cb2a7bea74433a90a47142849b1ea
Quellennotizuspto-grants-2008_09