Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445002Erstellt: 25. Oktober 2026

Hydrochloric Acid → tert-butyl 3-[4'-(2-Carboxy-ethyl)-biphenyl-4-yl]-propionate

https://huagongshe.com/reaction/445002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt4-(2-Carboxyethyl)benzeneboronic acidHCID 3863484—
EduktTert-butyl 3-(4-bromophenyl)propanoateHCID 10708234—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelAcetonitrile--water (1/1)HCID 18373917—
Produkttert-butyl 3-[4'-(2-Carboxy-ethyl)-biphenyl-4-yl]-propionateHCID 66724435—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Tert-butyl 3-(4-bromophenyl)propionate (433 mg, 1.52 mmol) in acetonitrile-water (3:1, 13 ml) under argon atmosphere was treated with 4-(2-carboxyethyl)benzeneboronic acid (294 mg, 1.52 mmol), K2CO3 (251 mg, 1.82 mmol) and (Ph3P)4Pd (87 mg, 73 μmol), and the stirred mixture was heated at 90° C. for 4 hours. Excess ethyl acetate and 2 M HCl was added and the organic phase was washed with 2×2 M HCl and 2× water. Drying over MgSO4 and evaporation in vacuo gave the crude product, which was purified by chromatography on silica column eluted with ethyl acetate/hexane/acetic acid 50:50:1 to provide tert-butyl 3-[4′-(2-Carboxy-ethyl)-biphenyl-4-yl]-propionate, 330 mg (62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476228B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-86ed1a602c25408da07f312c5cd6f566
Quellennotizuspto-grants-2013_07