HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 11470391, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 2-Naphthalenecarbonitrile | HCID 11944 | — |
| Reactant | 1-Octyne | HCID 12370 | — |
| Solvent | Benzonitrile | HCID 7505 | — |
| Product | HCID 11470391 | HCID 11470391 | 99% |
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 2-naphthonitrile (0.306 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 22 h at 65° C. showed the presence of 1.98 mmol (99% yield) of 2-(1-octynyl)naphthalene and no remaining 2-naphthonitrile 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-44b32b9f9a7c46e9ac8df5380d079e06 |
| Source note | uspto-grants-2006_09 |