HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 6-[4-(2-Oxopropoxy)phenyl]-4,5-dihydropyridazin-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-(4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone | HCID 135827540 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-[4-(2-Oxopropoxy)phenyl]-4,5-dihydropyridazin-3(2H)-one | HCID 14441854 | — |
Reaction Steps
A mixture of 4,5-dihydro-6-(p-hydroxyphenyl)-3(2H)pyridazinone (0.55 g), chloroacetone (0.32 g) and potassium carbonate (0.4 g), with a catalytic amount of potassium iodide, was stirred and heated under reflux in acetone (60 ml) for 16 hr. The solvent was evaporated and the residue partitioned between water and ethyl acetate. The organic layer was dried (MgSO4) and evaporated to a gum which was purified by chromatography on Silica gel. Elution with methanol-chloroform (4:96) gave 4,5-dihydro-6-(4-acetonyloxyphenyl)-3(2H)-pyridazinone as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153210 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-443f291e23b44c30b58574d54517d109 |
| Source note | uspto-grants-1992_10 |