HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroquinoline → 2-(4-Phenylbut-1-ynyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | 4-Phenyl-1-butyne | HCID 123360 | — |
| Product | 2-(4-Phenylbut-1-ynyl)quinoline | HCID 11594080 | 37% |
Reaction Steps
The title compound was prepared in accordance with the general method of Example 1, from 2-chloroquinoline (300 mg, 1.83 mmol) and 1-(but-3-ynyl)benzene (200 mg, 1.54 mmol). The crude residue was purified by flash chromatography (cyclohexane/AcOEt 95:5) to yield 148 mg (0.57 mmol, 37%) of 2-(4-phenylbut-1-ynyl)quinoline as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883826B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-b435edc753e945889c143c57f41cb8ac |
| Source note | uspto-grants-2014_11 |