HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308153Generated: November 2, 2026
Potassium Carbonate → 4-Methyl-2-phenylquinoline
https://huagongshe.com/reaction/2308153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-Chloro-4-methylquinoline | HCID 69449 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Methyl-2-phenylquinoline | HCID 20919 | 61% |
Reaction Steps
2-Chloro-4-methylquinoline (5.0 g, 30 mmol) and phenyl boronic acid (4.4 g, 36 mmol) were dissolved into 100 mL of ethylene glycol dimethyl ether. To the stirred reaction was added triphenylphosphine (0.8 g) and palladium(II) acetate, followed by 50 mL of a 2 M solution of potassium carbonate. The reaction was refluxed for 16 hours. After cooling, the aqueous layer was discarded and additional ethyl acetate added. The organics were washed with a saturated solution of sodium chloride and separated. The organic layer was dried over magnesium sulfate, concentrated, and purified on a silica gel column using 20% ethyl acetate and hexanes as the eluants. The pure fractions were combined and concentrated to give 2-phenyl-4-methylquinoline (4.0 g, 61% yield) as an oil.
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-e2cf8114536042a0951a2f81f871b771 |
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| Source note | uspto-grants-2004_12 |
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