HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → 1-chloro-4-(1-octynyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 4-Chlorobenzonitrile | HCID 12163 | — |
| Reactant | 1-Octyne | HCID 12370 | — |
| Catalyst | HCID 11748437 | HCID 11748437 | — |
| Solvent | Benzonitrile | HCID 7505 | — |
| Product | 1-chloro-4-(1-octynyl)benzene | HCID 10846604 | 70.5% |
Reaction Steps
The procedure was identical to Example 1, 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-chlorobenzonitrile (0.275 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 23 h at 65° C. showed the presence of 1.41 mmol (70% yield) of 1-chloro-4-(1-octynyl)benzene, 0.11 mmol 1,4-bis(1-octynyl)benzene and no remaining 4-chlorobenzonitrile 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-312db37ac42b4b2ab5e379071f40b6f9 |
| Source note | uspto-grants-2006_09 |