HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Buta-1,3-diynylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 1,3-Butadiyne | HCID 9997 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Product | Buta-1,3-diynylbenzene | HCID 11355482 | — |
Reaction Steps
The thus-obtained diacetylene derivative represented by the formula (IX) is then dissolved in benzene and refluxed while being heated for 30 min. to 1 hour in the presence of potassium hydroxide. After the reaction has been completed, the reaction mixture is filtered, and the solvent is then evaporated. The residure is then purified by silica-gel column chromatography to obtain a phenylbutadiyne derivative represented by the formula (X).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196586 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-ae9e4a22b0b243b4af96ec7dffa206fb |
| Source note | uspto-grants-1993_03 |