HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Allyl phenyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Mercurobutol | HCID 71633 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Product | Allyl phenyl ether | HCID 74458 | 92% |
Reaction Steps
More precisely, 9.3 g of mercurobutol are taken which are dissolved in 50 ml of hot denatured alcohol, in the presence of NaCl. 2 g of potash are carefully added. A thick white precipitate is formed. 4.4 ml of allyl bromide are added in 21 ml of denatured alcohol and the product is mixed with the precipitate which becomes more fluid. The product is heated for two hours at the boiling temperature of the alcohol, then filtered hot. 9.43 g of 2-chloromercuri 4-tertiobutyl phenol allyl-ether are obtained, with a yield of 92%. This product is pure, as may be checked by thin layer chromatography. Its melting temperature is 110° C. It is in the form of a white, water-insoluble powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931577 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-32cf2776ca1d4148b9e3406c93f88298 |
| Source note | uspto-grants-1990_06 |