HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanopyridine → HCID 11229223, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 1-Octyne | HCID 12370 | — |
| Solvent | Benzonitrile | HCID 7505 | — |
| Product | HCID 11229223 | HCID 11229223 | 80% |
Reaction Steps
The procedure was identical to Example 2, with the exception that 1-octyne (0.590 ml; 0.441 g; 4.00 mmol) was used as a substrate instead of phenylacetylene and 4-cyanopyridine (0.208 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 21 h at room temperature showed the presence of 1.60 mmol (80% yield) of 4-(1-octynyl)pyridine and no remaining 4-cyanopyridine in the reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105707B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-886c6ea6b49948b4bd3f9d6aeea1c775 |
| Source note | uspto-grants-2006_09 |