HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3-[4-(4-Chlorophenoxy)phenoxy]-1-propene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Chlorophenoxy)phenol | HCID 12346120 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 3-[4-(4-Chlorophenoxy)phenoxy]-1-propene | HCID 10491620 | 100.8% |
Reaction Steps
42 g of 4(4-chlorophenoxy)-phenol and 48 g of allyl bromide were heated at the boil at a reflux condenser, while stirring and adding 50 g of potassium carbonate, in 500 ml of butanol for 4 hours. Inorganic salts were then separated from the reaction solution by suction-filtration, the solvent was vaporized and the residue was distilled under greatly reduced pressure. 50 g of 4(4-chlorophenoxy)-phenyl allyl ether were obtained, boiling point: 173°-175° C. under a pressure of 2--3 mm mercury.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04301295 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-709bfe742ac242d39659ad02d703c88d |
| Source note | uspto-grants-1981_11 |