HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384396Generated: October 30, 2026
Water → Ethyl 4'-methoxy[1,1'-biphenyl]-4-carboxylate
https://huagongshe.com/reaction/1384396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 4-bromobenzoate | HCID 22043 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 4'-methoxy[1,1'-biphenyl]-4-carboxylate | HCID 2764348 | — |
Reaction Steps
A stirred mixture of 4-bromobenzoic acid, ethyl ester (23.6 g, 103 mmol), 4-methoxyphenylboronic acid (15.6 g, 103 mmol), tetrakis(triphenylphosphine)palladium (0) (2.0 g, 1.73 mmol) and powdered caesium fluoride (30.0 g, 200 mmol) in 1,2-dimethoxyethane (300 mL) is heated at 85° C. for 3 h. The mixture is then treated with water (500 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts are washed (saturated NaCl), dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by chromatography (silica gel, 5% ethyl acetate/95% cyclohexane) to 4′-methoxy-[1,1′-biphenyl]-4-carboxylic acid, ethyl ester as a colourless crystalline solid. m.p. 103-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258843B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-3d22307a24774ef295f6e00a72b50bb6 |
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| Source note | uspto-grants-2001_07 |
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