HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5-Trichlorophenol → HCID 12531851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5-Trichlorophenol | HCID 11859 | — |
| 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 | Potassium Iodide | HCID 4875 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12531851 | HCID 12531851 | — |
Reaction Steps
To a solution of 4.93 g of 3,4,5-trichlorophenol and 1.19 g of sodium methoxide 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 and 50 mg of potassium iodide. The mixture is refluxed for 20 hours and the solvent removed in vacuo. To the residue is added water and the mixture is extracted with ether. The ether extracts are washed with 10% potassium carbonate and with water and dried (MgSO4). Evaporation of the solvent under vacuum gives a tan oil. The oil is dissolved in chloroform and filtered through a column of silica gel. Removal of the solvent from the second 200 ml cut gives the product as a tan oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168385 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-61a057739ad14201a40aa486ccf675ea |
| Source note | uspto-grants-1979_09 |