HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 2-(4-chloro-3-methylphenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Methyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionate | HCID 12531902 | — |
| Reactant | Methyl (4-chloro-3-methylphenoxy)[p-(p-chlorophenoxy)phenyl]acetate | HCID 12531906 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(4-chloro-3-methylphenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionate | HCID 20392566 | — |
Reaction Steps
A solution of 0.015 mole of lithium N,N-diisopropylamide (prepared as in example 55) in tetrahydrofuran is chilled to -65° C to -75° C. To the solution is added methyl (4-chloro-3-methylphenoxy)[p-(p-chlorophenoxy)phenyl]acetate in tetrahydrofuran. To the mixture is added 5 ml of hex amethylphosphoramide and while chilling to -65° C to -75° C, 4.26 g of methyl iodide is added. After 1 hr., the mixture is allowed to warm to room temperature and stir overnight. The mixture is poured into water and extracted with ether. The ether extracts are washed with 10% hydrochloric acid, water, saturated NaHCo3, saturaed NaCl solution and dried (MgSO4). Evaporation of the solvent under reduced pressure gives the product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125729 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-27967b1bd6f742859a95b742a87f3d5e |
| Source note | uspto-grants-1978_11 |