HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Methyl (m-[m-phenoxyphenoxy]phenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phenol, 3-(3-phenoxyphenoxy)- | HCID 84251 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 20392594 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl (m-[m-phenoxyphenoxy]phenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 86736645 | — |
Reaction Steps
To a solution of 6.96 g of m-(m-phenoxyphenoxy)phenol, 1.19 g of sodium methoxide and 50 mg of potassium iodide in 40 ml of methanol is added 7.11 g of methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The mixture is refluxed for 20 hours, poured into ice and water and extracted with chloroform. The chloroform extracts are washed with 10% potassium carbonate and with water. The extract is dried over magnesium sulfate and concentrated under vacuum to give an oil. Filtration once through silica gel (chloroform solvent) and again through silica gel with benzene as solvent gives the product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168385 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-bda675eb7dbd4415a813c129aea4875b |
| Source note | uspto-grants-1979_09 |