HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-(ALLYLOXY)BENZONITRILE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(ALLYLOXY)BENZONITRILE | HCID 257949 | 96% |
Reaction Steps
A mixture comprising 29.75 g of 4-cyanophenol, 33.27 g of allyl bromide, 41.46 g of potassium carbonate and 350 ml of acetone, was refluxed under stirring for 4 hours. Acetone was distilled, and water was added to the residue. The mixture was extracted with benzene. The benzene layer was washed sequentially with a 5% sodium hydroxide aqueous solution and water, and dried over sodium sulfate. Then, the solvent was distilled off to obtain a pale yellow oily substance. The residual substance was crystallized from n-hexane-ethyl ether to obtain 38.16 g of 4-allyloxy benzonitrile as colorless crystals having a melting point of from 40.5° to 41° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04783462 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-394c0f2782b044788ba171e7aa87b880 |
| Source note | uspto-grants-1988_11 |