HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4,6-Diphenyl-4,5-dihydropyridazin-3(2h)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Phenyl-6-pyridazone | HCID 75106 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,6-Diphenyl-4,5-dihydropyridazin-3(2h)-one | HCID 283915 | 50% |
Reaction Steps
135 ml (135 mmole) of a solution of phenylmagnesium bromide (1M) in THF was added to a hot suspension of 6-phenylpyridazinone compound 7.8 g (45 mmole) in dry toluene (50 ml). The mixture was refluxed for 8 h, left overnight at ambient temperature, then decomposed with a saturated solution of ammonium chloride. The organic layer was separated, and the aqueous layer was extracted with 100 ml of ethyl acetate. The solvent was removed and the residue was crystallized from ethanol. The crystals were collected by filtering and dried over a medium frit sintered glass funnel in vacuo to give 5.6 g of white crystals. Yield was 50%, confirmed by ESI-MS. ESI-MS: m/z 250.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158627B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-9f70c175c7c747ef88a26a3795e8f525 |
| Source note | uspto-grants-2012_04 |