HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Di-(2-propenylphenoxy) methane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 2-Propenylphenol | HCID 93029 | — |
| Product | Di-(2-propenylphenoxy) methane | HCID 57173787 | — |
Reaction Steps
The preparation of 2-propenylphenol from phenol and allyl bromide is similar to that outlined1. The reaction of this compound with dibromomethane is similar to that described above for di (N-phenylcarboxaldimine-4-phenoxy)methane. The title compound was extracted with ether 3×100 ml portions from the aqueous dimethylformamide solution, washed with aqueous potassium hydroxide (10%) and then water. The ether phase was dried over sodium sulphate and the solvent was stripped off under reduced pressure. The oil which contained some (~5%) of a less polar component and at least two isomeric forms of the title compound, as indicated from high pressure liquid chromatography, was used without further purification in the reaction below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05001294 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-35b23179de3e4e17a12734ba84fc7665 |
| Source note | uspto-grants-1991_03 |