HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzonitrile → Benzene, 1-methyl-4-(phenylethynyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | p-Ethynyltoluene | HCID 13018 | — |
| Product | Benzene, 1-methyl-4-(phenylethynyl)- | HCID 3014187 | 81% |
Reaction Steps
The procedure was identical to Example 1, with the exception that 4-ethynyltoluene (0.507 ml; 0.465 g; 4.00 mmol) was used as a substrate instead of phenylacetylene. GC analysis of the organic phase of the hydrolyzed reaction sample after 42 h at 65° C. showed the presence of 1.62 mmol (81% yield) of 1-methyl-4-(phenylethynyl)benzene, and 0.25 mmol of benzonitrile remaining 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-6ef020ade22348b8a18215c8077c6abe |
| Source note | uspto-grants-2006_09 |