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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437272Generated: November 2, 2026

Dimethyl oxalate → Methyl 4-(3-pyridazinyl)-2,4-dioxobutanoate

https://huagongshe.com/reaction/1437272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl oxalateHCID 11120—
Reactant1-(Pyridazin-3-yl)ethan-1-oneHCID 352755—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(3-pyridazinyl)-2,4-dioxobutanoateHCID 23143718—

Reaction Conditions

Temperature-78 °C

Reaction Steps

In an argon atmosphere and while cooling at −78° C., 1.0M lithium bis(trimethylsilyl)amide in tetrahydrofuran (19 mL) was added dropwise to 3-acetylpyridazine (2.097 g) in tetrahydrofuran (50 mL), followed by stirring for 1 hour. To the reaction mixture, dimethyl oxalate (4.055 g) in tetrahydrofuran (35 mL) was added dropwise, and the resultant mixture was stirred at 0° C. for 2 hours. The reaction solvent was removed under reduced pressure. Water was added to the residue, and the mixture was washed with diethyl ether. The aqueous layer was slightly acidified with aqueous 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried over sodium sulfate anhydrate, followed by filtration. The solvent was removed under reduced pressure, to thereby give 4-(3-pyridazinyl)-2,4-dioxobutanoic acid methyl ester as a solid (2.63 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622471B2
Source datasetuspto-grants-2009_11
ORD IDord-52ac3b00bd124d8591cbb77b5f1e72c0
Source noteuspto-grants-2009_11