HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Ethyl Ketone → 4-(4-Prop-2-enoxyphenyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| 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 | 91.3% |
Reaction Steps
A solution prepared by adding 20 g of 4-cyano-4′-hydroxybiphenyl, 20 g of allyl bromide and 25 g of potassium carbonate to 250 ml of 2-butanone was refluxed for 7 hours. Water was added to the reaction solution for liquid-liquid separation, and the organic layer was washed with water and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the resulting residue was purified through silica gel column chromatography using toluene as an eluent solvent and then further recrystallized from ethanol to obtain 22 g of 4-allyloxy-4′-cyanobiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07541071B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-d7eac201409d43deb09cba2b530eecf4 |
| Source note | uspto-grants-2009_06 |