HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Methyl alpha-(3,5-di-tert-butylphenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| 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 | — |
| Product | Methyl alpha-(3,5-di-tert-butylphenoxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 12531858 | — |
Reaction Steps
To a solution of 5.16 g of 3,5-di-tert-butylphenol 1.188 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 solution is heated at reflux overnight and worked up as described in Example 70 to yield a yellos oil which is purified by chromatography on 100 of silica gel (benzene, 400 ml) and pumped in vacuo at 120° C. (0.05 mm) to yield a yellow glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168385 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-ab4db61f2a494946b017ff014304c1fd |
| Source note | uspto-grants-1979_09 |