HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(ALLYLOXY)BENZONITRILE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(ALLYLOXY)BENZONITRILE | HCID 257949 | 100% |
Reaction Steps
4-Hydroxybenzonitrile (30.0 g, 252 mmol), allyl bromide (39.6 g, 327 mmol), and Cs2CO3 (98.5 g, 302 mmol) were dissolved in DMF (900 mL), and water (1 mL) was added. After stirring for 12 h at rt, the reaction mixture was concentrated under reduced pressure, water was added, and the mixture was extracted with EtOAc (2×). The combined organic layers were washed with water and brine. The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure yielding 40 g (100%) of the title compound as a white crystalline solid. 1H NMR (400 MHz, CDCl3): δ 4.60 (d, 2H), 5.34 (d, 1H), 5.43 (d, 1H), 6.03 (m, 1H), 6.96 (d, 2H), 7.58 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714004B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-a3a6e0a5bf2445cfbbb8f01b8a95a71a |
| Source note | uspto-grants-2010_05 |