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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264599Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-(n-Pentoxyphenyl)-4'-carboxybiphenyl

https://huagongshe.com/reaction/264599

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium CarbonateHCID 10340—
Edukt4-Iodobenzoic acidHCID 12085—
Edukt4'-Pentyloxybiphenyl-4-boronic AcidHCID 11358071—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
Produkt4-(n-Pentoxyphenyl)-4'-carboxybiphenylHCID 2147955070,9%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a stirred mixture of 4-(4-n-pentoxyphenyl)phenylboronic acid (1.0 g, 3.52 mmol) and 4-iodobenzoic acid (874 mg, 3.52 mmol) in ethanol (11 ml) and toluene (30 ml) was added an aqueous solution of sodium carbonate (2M, 5.3 ml, 10.6 mmol) followed by tetrakis(triphenylphosphine)palladium (204 mg, 5 mol %). The reaction mixture was heated at 100° C. under a nitrogen atmosphere for a period of 18 h. The cooled mixture was acidified to pH 3 (1N HCl) and partitioned between ethyl acetate and water. The organic phase was washed with water (3×) and brine, dried with magnesium sulfate, and filtered through a bed of Celite. The solvent was removed in vacuo to give crude product which was purified by flash silica gel chromatography to provide 4-(n-pentoxyphenyl)-4'-carboxybiphenyl (450 mg): 1H NMR (400 MHz, DMSO-d6) δ0.89 (t, 3H), 1.37 (m, 4H), 1.72 (m, 2H), 3.98 (t, 2H), 7.01 (d, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646245
Quelldatensatzuspto-grants-1997_07
ORD IDord-0ab78d509caa495cabb27b4ae2337c97
Quellennotizuspto-grants-1997_07