HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992264Generated: October 30, 2026
Ethylene Glycol → HCID 18412020, compound
https://huagongshe.com/reaction/992264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 18412002 | HCID 18412002 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18412020 | HCID 18412020 | 89.4% |
Reaction Steps
A suspension of 6-acetyl-4-bromo-2-(4-fluorophenyl)-5-methyl-3(2H)-pyridazinone (3.2 g), ethylene glycol (3.1 g) and p-toluenesulfonic acid (0.2 g) in toluene (35 ml) was heated under reflux for 10 hours with removing water formed. After cooling on standing, the reaction mixture was extracted with ethyl acetate. After washing with a saturated aqueous sodium hydrogen carbonate solution and a brine, the organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by evaporation, the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2), and the resulting crude crystals were washed with hexane to obtain 4-bromo-2-(4-fluorophenyl)-5-methyl-6-(2-methyl-1,3-dioxolan-2-yl)-3(2H)-pyridazinone (3.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469003B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3dde0a3dc2364b2cbdf014e8df4d5f00 |
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| Source note | uspto-grants-2002_10 |
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