HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → 1-fluoro-4-(1-octynyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 1-Octyne | HCID 12370 | — |
| Reactant | 4-Fluorobenzonitrile | HCID 14517 | — |
| Solvent | Benzonitrile | HCID 7505 | — |
| Product | 1-fluoro-4-(1-octynyl)benzene | HCID 10899731 | 67% |
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-fluorobenzonitrile (0.242 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 45 h at 65° C. showed the presence of 1.34 mmol (67% yield) of 1-fluoro-4-(1-octynyl)benzene and no remaining 4-fluorobenzonitrile 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-da53e74c167b43d482bb343abe71cd84 |
| Source note | uspto-grants-2006_09 |