HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → 4-(4-Prop-2-enoxyphenyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-Hydroxy-4-biphenylcarbonitrile | HCID 140610 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Prop-2-enoxyphenyl)benzonitrile | HCID 2341987 | — |
Reaction Steps
A reaction mixture obtained by adding 20 g of 4-cyano-4′-hydroxybiphenyl, 20 g of ally bromide and 25 g of potassium carbonate to 250 mL of butanone was refluxed for 7 hours. Water was added to the reaction mixture, which was then separated. An organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain a residue, which was purified by silica gel column chromatography using toluene as an elusion solvent and then subjected to recrystallization from ethanol to obtain 22 g of 4-allyloxy-4′-cyanobiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07527746B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f839fe5bb4354ca6ac278e5ae858b7ab |
| Source note | uspto-grants-2009_05 |