HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-(Bromomethyl)-2-cyanobiphenyl → 2-Cyano-4'-methylbiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-(Bromomethyl)-2-cyanobiphenyl | HCID 1501912 | — |
| Reactant | 4'-(Dibromomethyl)[1,1'-biphenyl]-2-carbonitrile | HCID 11100227 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Cyano-4'-methylbiphenyl | HCID 145512 | — |
Reaction Steps
After the dropwise addition of the solution prepared by dissolving the mixture of 4'-dibromomethyl-2-cyanobiphenyl and 4'-bromomethyl-2-cyanobiphenyl in toluene was terminated, the mixture was allowed to react up to a point where the above suspension no longer absorbs hydrogen gas. After the reaction was terminated, Raney catalyst and sodium carbonate were filtered off, and the reaction mixture was then concentrated to distill off methanol and toluene. The resulting crude 4'-methyl-2-cyanobiphenyl was purified by distillation, to give 7.4 g of 4'-methyl-2-cyanobiphenyl having an LC purity of 98.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05892094 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-aa50b0f8aff3430c92ea45fe2186bb22 |
| Source note | uspto-grants-1999_04 |