HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895075Generated: October 30, 2026
Carbon Dioxide → 4-Acetyl-2-(2'-hydroxyethyl)-5,6-bis(4-chlorophenyl)-2H-pyridazin-3-one
https://huagongshe.com/reaction/895075
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 75643-31-1 | HCID 439087 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Acetyl-2-(2'-hydroxyethyl)-5,6-bis(4-chlorophenyl)-2H-pyridazin-3-one | HCID 100711 | 68% |
Reaction Steps
4-Acetyl-5,6-bis(p-chlorophenyl)-2H-pyridazin-3-one (3.1 g), ethylene carbonate (2.0 g), and potassium hydroxide (powdered) were dissolved in dimethylformamide (50 ml) and the flask placed in an oil bath (110°-120° C.) until CO2 evolution ceased (ca. 3.5 hours). The reaction mixture was poured into water (400 ml) and chilled at 5° C. for 1 hour. The resulting precipitate was separated by filtration and recrystallized from methanol (85 ml) to afford 4-acetyl-5,6-bis(p-chlorophenyl)-2-(2'-hydroxyethyl)-2H-pyridazin-3-one (68 percent yield) as pale yellow crystals, m.p. 191°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04286091 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-af94b3bd2ae64990ba576542d4724beb |
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| Source note | uspto-grants-1981_08 |
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