HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 2,5-Bis(4-cyanophenyl)furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 19977168 | HCID 19977168 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2,5-Bis(4-cyanophenyl)furan | HCID 622985 | 68% |
Reaction Steps
A mixture of 2,5-bis(4-bromophenyl)-3-furan carboxylic acid 0.85 g (0.002 mole), CuCN 0.45 g (0.005 mole) in 10 ml freshly distilled quinoline is heated under reflux for 3 hours. The mixture is cooled and 100 ml dilute aqueous HCl is added and the mixture is stirred for 30 min. and filtered. The solid is washed with water and then with hexane. The resultant yellow solid is dissolved in acetone and passed through an alumina (neutral) column to yield a yellow crystalline solid 0.37 g (68%) having amp of 293°-295° C. The product is identical with that described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05602172 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-783162db3dff460eb7812e83cb60089d |
| Source note | uspto-grants-1997_02 |