HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-(2,4-Dichlorophenoxy)-3-(2-oxopropoxy)-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 25023955 | HCID 25023955 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(2,4-Dichlorophenoxy)-3-(2-oxopropoxy)-benzonitrile | HCID 68614765 | — |
Reaction Steps
21.56 g of 4-(2,4-dichlorophenoxy)-3-hydroxybenzonitrile, 14.2 g of chloroacetone, 12.8 g of potassium carbonate and 170 mg of potassium iodide are dissolved in 300 ml of acetone and boiled under reflux for 5 h. After cooling, the precipitate is filtered, concentrated by evaporation, redissolved in ethylacetate and washed with a 1N aqueous solution of sodium hydroxide, water, a 1N aqueous solution of hydrogen chloride and finally with brine. The organic phase is dried over magnesium sulfate and evaporated. The residue is recrystallized from ethylacetate/hexane to yield 4-(2,4-dichlorophenoxy)-3-(2-oxopropoxy)-benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705047B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-8ae83f0512bd44e5bf4dc21545d32d88 |
| Source note | uspto-grants-2010_04 |