HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 4-Methoxy-3-fluoro-4"-cyano-p-terphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4'-bromo-[1,1'-Biphenyl]-4-carbonitrile | HCID 1394462 | — |
| Reactant | 3-Fluoro-4-methoxyphenylboronic acid | HCID 2782194 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methoxy-3-fluoro-4"-cyano-p-terphenyl | HCID 22079629 | 88.6% |
Reaction Steps
To a mixture of 2.4 g of 4-bromo-4'-cyanobiphenyl, 0.37 g of tetrakis(triphenylphosphine)palladium(0), 15.2 ml of a 2N aqueous sodium carbonate solution, and 19.4 ml of benzene, a solution which was prepared by dissolving 1.9 g of 4-methoxy-3-fluoro-benzene boronic acid synthesized in [1] above in 14.4 ml of ethanol was slowly added dropwise with stirring, and the solution was subjected to reflux for 8 hours. After the reflux was finished, the solution was cooled, and the crystals thus precipitated were separated by filtration and washed with water and methanol in turn, and dried to obtain 2.5 g of 4-methoxy-3-fluoro-4"-cyano-p-terphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05417885 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-856c078c427a48308a9a01c4b78b789f |
| Source note | uspto-grants-1995_05 |