HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 57057502, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 3533755 | HCID 3533755 | — |
| Reactant | HCID 11171268 | HCID 11171268 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 57057502 | HCID 57057502 | — |
Reaction Steps
O-propenylphenol (67 g) was added to a stirred suspension of potassium carbonate (138 g) in dry acetone. Allyl bromide (67 g) was then added dropwise over about 20 minutes and the stirred mixture was heated under reflux for 4 hours. After this time, gas liquid chromatography indicated that the phenol had been converted to about 95% of a mixture of cis and trans 2-allyloxy-1-propenylbenzene. The mixture was filtered and the solvent removed under reduced pressure. The residue was vacuum distilled and yielded 58.9 g of almost pure 2-allyloxy-1-propenylbenzene which was identified spectroscopically. [b.p. 64-88° C. at 0.6 mbar].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05021512 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-3de632b9268c44fa87b847a46594feba |
| Source note | uspto-grants-1991_06 |