HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-(ALLYLOXY)BENZONITRILE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(ALLYLOXY)BENZONITRILE | HCID 257949 | — |
Reaction Steps
A solution of 4-cyanophenol (50 g), allyl bromide (27.2 ml) potassium carbonate (47.8 g) in acetone (100 ml) was heated at reflux for 16 hours. The reaction mixture was evaporated, water was added to the residue and the aqueous mixture was extracted with diethyl ether. The diethyl ether extract was washed with dilute aqueous sodium hydroxide solution, dried (MgSO4) and evaporated to give 4-cyanophenyl allyl ether as a solid, m.p. 41.6° C.; microanalysis, found: C, 75.1; H, 5.8; N, 8.7%; C10H9NO2 requires: C, 75.5; H, 5-7; N, 8.8%; NMR: 4.55-4.65(2H,m), 5.2-5.4(2H,m), 5.9-6.05(1H,m), 7.0-7.1(2H,m) and 7.65-7.75(2H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05691349 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-f2b8299f0996402c9b9d11ec0351f35c |
| Source note | uspto-grants-1997_11 |