HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-3-methylphenol → Methyl (4-chloro-3-methylphenoxy)[p-(p-chlorophenoxy)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-3-methylphenol | HCID 1732 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| 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 (4-chloro-3-methylphenoxy)[p-(p-chlorophenoxy)phenyl]acetate | HCID 12531906 | — |
Reaction Steps
To a solution of 3.565 g of 4-chloro-3-methylphenol, 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 mixture is refluxed overnight and poured into 100 ml of water. The mixture is extracted with 2×75 ml of ether and the combined extracts are washed with 50 ml of 5% NaOH, 50 ml of water, 50 ml of saturated brine and dried (MgSO4). Evaporation of the solvent yields a yellow oil. Chromatography on 100 g of silica gel yields a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168385 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-7985208701084316a532e3ad212ab10e |
| Source note | uspto-grants-1979_09 |