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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1,3-Diethyl 2-oxopropanedioateHCID 69105—
Reactant1-(Benzofuran-5-yl)ethanoneHCID 18693752—
SolventIsopropanolHCID 3776—
Product6-(1-benzofuran-5-yl)-4-carboxy-2H-pyridazin-3-oneHCID 23094110—

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314877B2
Source datasetuspto-grants-2008_01
ORD IDord-017e90636fa94908a46b0d4de27df207
Source noteuspto-grants-2008_01