HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511477Generated: November 3, 2026
Potassium Carbonate → Ethyl 4-ethoxy-2,3-difluoro-4'-biphenylcarboxylate
https://huagongshe.com/reaction/1511477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | B-(4-Ethoxy-2,3-difluorophenyl)boronic acid | HCID 15135235 | — |
| Reactant | Ethyl 4-iodoethylbenzoate | HCID 66963157 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4-ethoxy-2,3-difluoro-4'-biphenylcarboxylate | HCID 66962505 | 74.7% |
Reaction Steps
Ethyl 4-iodoethylbenzoate (1) (25.0 g), 4-ethoxy-2,3-difluorophenylboronic acid (2) (20.1 g), potassium carbonate (25.0 g), Pd/C (0.25 g), toluene (100 ml), ethanol (100 ml) and water (100 ml) were put in a reaction vessel under a nitrogen atmosphere, and heated under reflux for 2 hours. The reaction mixture was cooled to 25° C., and then poured into water (500 ml) and toluene (500 ml), and mixed. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases. The extraction to an organic phase was carried out. The organic phase obtained was washed with water, and then dried over anhydrous magnesium sulfate. The solution obtained was concentrated under reduced pressure, and the residue obtained was purified by means of column chromatography (silica gel; toluene). The product was further purified by means of recrystallization from ethanol and dried, giving 18.8 g of ethyl 4-ethoxy-2,3-difluoro-4′-biphenylcarboxylate (3). The yield based on the compound (1) was 67.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08216489B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-2e055dfe50b24da982e00080b7d70ade |
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| Source note | uspto-grants-2012_07 |
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