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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129799Generated: October 25, 2026

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

https://huagongshe.com/reaction/129799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-butylbenzeneHCID 521059—
ReactantEthyl 3-(4-iodophenyl)propanoateHCID 15661143—
ReactantHCID 178418306HCID 178418306—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4'-Butyl[1,1'-biphenyl]-4-propanoic acid, ethyl esterHCID 8674912291%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05470845
Source datasetuspto-grants-1995_11
ORD IDord-cedff70d1be44213affec8bec8a653d4
Source noteuspto-grants-1995_11