HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 11217767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 4-Chlorobenzonitrile | HCID 12163 | — |
| Reactant | 1-Hexyne | HCID 12732 | — |
| Catalyst | HCID 11831501 | HCID 11831501 | — |
| Solvent | Benzonitrile | HCID 7505 | — |
| Product | HCID 11217767 | HCID 11217767 | 65% |
Reaction Steps
The procedure was identical to Example 2, with the exception that 1-hexyne (0.450 ml; 0.329 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 20 h at 65° C. showed the presence of 1.29 mmol (65% yield) of 1-chloro-4-(1-hexynyl)benzene, 0.10 mmol 1,4-bis(1-hexynyl)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-d9a3b0de11cb4ccf8303f120daa1260a |
| Source note | uspto-grants-2006_09 |