HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17759Generated: October 26, 2026
Potassium Carbonate → HCID 58704556, compound
https://huagongshe.com/reaction/17759
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-6-methylquinoline | HCID 77974 | — |
| Reactant | 3-Methylphenylboric acid | HCID 22237835 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58704556 | HCID 58704556 | — |
Reaction Steps
3-methyl-phenyl-boric acid (1.3 mmol), 2-chloro-6-methyl-quinoline (1 mmol), tetrakis(triphenyl phosphine) palladium(0) (0.05 mmol), and potassium carbonate (3 mmol) are dissolved in a two-neck round bottom flask containing THF (30 ml) and H2O (10 ml). The mixture is then stirred for 24 hours in a bath of 100 degrees Celsius (C). Subsequently, when reaction no longer occurs, the THF and toluene are discarded. The mixture is extracted by using dichloromethane and water, which is then treated with vacuum distillation. Then, after filtering the mixture with a silica gel column, a solvent is treated with vacuum distillation. Thereafter, by using dichloromethane and petroleum ether, the mixture is re-crystallized and filtered, thereby yielding solid 2-(3-methylphenyl)-6-methyl-quinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07740957B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-ec77232869994d2980a45ec9a09d6335 |
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| Source note | uspto-grants-2010_06 |
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