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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273401Erstellt: 25. Oktober 2026

Water → Methyl 3-[4-[(4'-chloro-2'-methylbiphenyl-3-yl)methoxy]phenyl]propanoate

https://huagongshe.com/reaction/273401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt(4-Chloro-2-methylphenyl)boronic acidHCID 5017600—
EduktMethyl 4-[(3-bromophenyl)methoxy]benzenepropanoateHCID 23136270—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 3-[4-[(4'-chloro-2'-methylbiphenyl-3-yl)methoxy]phenyl]propanoateHCID 5890315088,5%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of methyl 3-[4-[(3-bromobenzyl)oxy]phenyl]propanoate (0.5 g, 1.43 mmol), 4-chloro-2-methylphenylboronic acid (0.30 g, 1.72 mmol), tetrakis(triphenylphosphine)palladium(0) (0.083 g, 0.072 mmol), sodium carbonate (0.46 g, 4.29 mmol), water (5 mL), ethanol (5 mL) and toluene (25 mL) was stirred under an argon atmosphere at 90° C. for 16 hrs. The reaction mixture was cooled, diluted with ethyl acetate, washed with water and saturated brine, dried and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-4/1) to give the title compound (0.50 g, yield 88%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456218B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-cbe6b4fbe9b945ec9dd0c15d5272c25b
Quellennotizuspto-grants-2008_11