HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308152Generated: October 31, 2026
Potassium Carbonate → HCID 21044146, compound
https://huagongshe.com/reaction/2308152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | 2,4-Difluorophenylboronic acid | HCID 2734334 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 21044146 | HCID 21044146 | 98.6% |
Reaction Steps
2-Chloroquinoline (1.20 g, 12.2 mmol), 2,4-difluorophenylboronic acid (2.32 g, 14.7 mmol), were added to 10 mL of ethylene glycol dimethyl ether (DME) and 12 mL of a 2 M solution of potassium carbonate. Triphenylphosphine (0.32 g, 1.2 mmol) and palladium acetate (0.069 g, 0.3 mmol) were added to the stirred reaction mixture and refluxed for 17 hours under a nitrogen atmosphere. The mixture was cooled to room temperature and the aqueous phase was separated from the organic phase. The aqueous phase was extracted with 2×30 mL of ethyl acetate. The combined organic extracts were washed first with distilled water followed by brine. The solvent was dried over magnesium sulfate and concentrated to give 2-(2,4-difluorophenyl)quinoline (2.9 g, 98.6%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06835469B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-b93c2d48aadf4d96a64cc06c9165d183 |
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| Source note | uspto-grants-2004_12 |
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