HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-(2,3-Difluoro-6-nitrophenoxy)propan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Difluoro-6-nitrophenol | HCID 2733745 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(2,3-Difluoro-6-nitrophenoxy)propan-2-one | HCID 1268241 | 65.3% |
Reaction Steps
5.8 g of 2,3-difluoro-6-nitrophenol, 5.0 g of monochloroacetone, 8.0 g of potassium carbonate and 0.8 g of potassium iodide were added to 100 ml of acetone and the mixture was refluxed for 4 hours. After the removal of insoluble material by filtration, the solvent was evaporated and the residue was distributed between chloroform and water. The chloroform layer was washed with water and was dried, then the solvent was evaporated. The residue was treated with n-hexane to provide 5.0 g of 2-acetonyloxy-3,4-difluoronitrobenzene as light yellow crystals with m.p. 61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382892 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-6fb2dfaa0e1c49c2aa2f8266807d0b80 |
| Source note | uspto-grants-1983_05 |