HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 11298050, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 1-Hexyne | HCID 12732 | — |
| Reactant | 2-Furonitrile | HCID 69245 | — |
| Solvent | Benzonitrile | HCID 7505 | — |
| Product | HCID 11298050 | HCID 11298050 | 69% |
Reaction Steps
The procedure was identical to Example 1, with the exception that 1-hexyne (0.450 ml; 0.329 g; 4.00 mmol) was used as a substrate instead of phenylacetylene and 2-furonitrile (0.175 ml; 0.186 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 4 h at 65° C. showed the presence of 1.38 mmol (69% yield) of 2-(1-hexynyl)furan and no remaining 2-furonitrile 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-a2f8a0b8af5f4f7a82db255b25d6d2d2 |
| Source note | uspto-grants-2006_09 |