HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249426Generated: October 26, 2026
Hydrochloric Acid → 6-(1-benzofuran-5-yl)-4-carboxy-2H-pyridazin-3-one
https://huagongshe.com/reaction/2249426
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1,3-Diethyl 2-oxopropanedioate | HCID 69105 | — |
| Reactant | 1-(Benzofuran-5-yl)ethanone | HCID 18693752 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-(1-benzofuran-5-yl)-4-carboxy-2H-pyridazin-3-one | HCID 23094110 | — |
Reaction Steps
5-Acetyl-1-benzofuran (536 mg, 3.35 mmol) and diethyl ketomalonate (642 mg, 3.69 mmol) were mixed together, and the mixture was stirred for 34 hours at 120° C. Hydrazine monohydrate (247 mg, 4.93 mmol) was added to a solution of the reaction mixture in isopropanol (8.5 mL), and the resultant mixture was heated with stirring for six hours at 100° C. A 2-mol/L aqueous sodium hydroxide solution (5.2 mL) was added thereto, and the mixture was further stirred for four hours at 100° C. The mixture was cooled with ice, and concentrated hydrochloric acid was added thereto, to thereby acidify the heated system. The formed precipitates were collected through filtration, thoroughly washed with water, and dried, to thereby yield 397 mg of the title compound as a yellow powder (46.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314877B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-017e90636fa94908a46b0d4de27df207 |
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| Source note | uspto-grants-2008_01 |
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