Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Isoquinoline, 1-chloro- | HCID 140539 | — |
| Solvent | Dimethyl ether ethylene glycol | HCID 21863332 | — |
| Product | 1-Phenylisoquinoline | HCID 137882 | 90% |
Reaction Steps
3.0 g of 1-chloro-isoquinoline (18 mmmol), 2.7 g of Phenyl boronic acid (21 mmol), 1.6 g of tetrakis-triphenylphosphine palladium (0.8 mmol %), and 2.9 g of potassium carbonate (21 mmol) were added into 100 ml of reaction bowl, and 50 ml of ethylene glycol-dimethyl ether as distilled solvent was added thereto under the flow of nitrogen, and then the reaction was performed in reflux at 90° C. for 12 hr. The mixture was cooled to room temperature, extracted by chloroform and distilled water, and then, separated by silica gel column chromatography (chloroform:hexane=1:3), to obtain 3.32 g of 1-phenyl-isoquinoline (yield: 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442448B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-9f8c8816ff8448408184d0b77f719359 |
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| Source note | uspto-grants-2008_10 |
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