HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Methyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Methyl(p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetate | HCID 12531843 | — |
| Reactant | Methyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]propionate | HCID 12531902 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(p-chlorophenoxy)-2-[p-(p-chlorophenoxy)phenyl]butyrate | HCID 20392631 | — |
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 (p-chlorophenoxy)[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of tetrahydrofuran. To the mixture is added 5 ml of hexamethylphosphoramide and while chilling to -65° C. to -75° C., 4.68 g of ethyl iodide is added. After 1 hr., the mixture is allowed to warm to room temperature and stirr overnight. The mixture is poured into water and extracted with ether. The ether extracts are washed with 10% hydrochloric acid, water, saturated NaHCo3, saturated NaCl solution and dried (MgSO4). Evaporation of the 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-17e1205b157a4a7d855937b538b226d9 |
| Source note | uspto-grants-1979_09 |