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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-butylbenzene | HCID 521059 | — |
| Reactant | Ethyl 3-(4-iodophenyl)propanoate | HCID 15661143 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Butyl[1,1'-biphenyl]-4-propanoic acid, ethyl ester | HCID 86749122 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05470845 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-cedff70d1be44213affec8bec8a653d4 |
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| Source note | uspto-grants-1995_11 |
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