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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | 1-(Pyridazin-3-yl)ethan-1-one | HCID 352755 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(3-pyridazinyl)-2,4-dioxobutanoate | HCID 23143718 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622471B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-52ac3b00bd124d8591cbb77b5f1e72c0 |
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| Source note | uspto-grants-2009_11 |
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