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HRID 129799Erstellt: 24. Oktober 2026

1-Bromo-4-butylbenzene → 4'-Butyl[1,1'-biphenyl]-4-propanoic acid, ethyl ester

https://huagongshe.com/de/reaction/129799

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-butylbenzeneHCID 521059—
EduktEthyl 3-(4-iodophenyl)propanoateHCID 15661143—
EduktHCID 178418306HCID 178418306—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4'-Butyl[1,1'-biphenyl]-4-propanoic acid, ethyl esterHCID 8674912291%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 3.20 g (15.0 mmol) of 1-bromo-4-butylbenzene (Aldrich Chemical Company #33,576-2) at -78° C. under argon was added, dropwise over 30 min, 18.0 mL (30.6 mmol, 1.7M in pentane) of t-butyllithium solution. The resulting light yellow solution was warmed to 0° C. and stirred for 1 h. To this solution was added 3.4 g (25 mmol) of thrice-fused zinc chloride in 20 mL of THF. The resulting slurry was stirred for 30 min and then a solution of 2.0 g (6.5 mmol) of 4-iodobenzenepropanoic acid, ethyl ester (Example 43, Part B) and 0.4 g (0.35 mmol) of tetrakis(triphenylphosphine)palladium (0) in 5 mL of THF was added. The reaction was stirred for 16 h, diluted with ether and washed once with 10% citric acid. The organic phase was dried (MgSO4) and evaporated. Purification by flash chromatography on silica gel (5×20 cm column) eluted with 1:1 hexanes/dichloromethane gave title compound as a colorless oil, 1.79 g , 91% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05470845
Quelldatensatzuspto-grants-1995_11
ORD IDord-cedff70d1be44213affec8bec8a653d4
Quellennotizuspto-grants-1995_11