HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446891Generated: October 29, 2026
Sodium Chloride → HCID 68975311, compound
https://huagongshe.com/reaction/446891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Reactant | HCID 68975878 | HCID 68975878 | — |
| Reactant | HCID 68976696 | HCID 68976696 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 68975311 | HCID 68975311 | 49% |
Reaction Steps
Diethylmalonate (1.73 g, 1.64 mL, 2.5 eq) was dissolved in isopropyl ether (2 mL), sodium ethoxide (0.73 g, 2.5 eq) was added thereto at room temperature, and the mixture was stirred for 30 min. To the reaction mixture was added the compound of Preparation 3-1) (1.10 g, 4.31 mmol), which was then refluxed for one day. The mixture was extracted with ethyl acetate (50 mL×2), washed with aqueous sodium chloride solution (100 mL), dried (anhydrous Na2SO4), and concentrated under reduced pressure. The residue was separated by column chromatography (10-20% ethyl acetate-hexane) to give 1.34 g (82%) of a 1:1 mixture of 2-(2-benzyl-5-chloro-3-oxo-2,3-dihydro-pyridazin-4-yl)-malonic acid diethyl ester and 2-(1-benzyl-5-chloro-6-oxo-1,6-dihydro-pyridazin-4-yl)-malonic acid diethyl ester. This mixture was dissolved in 12 mL of a solvent mixture (H2O:DMSO=1:5), NaCl (1.0 g, 5 eq) was added thereto, and the mixture was heated to 120° C. for one day. The mixture was concentrated under reduced pressure, and the residue was extracted twice with ethyl acetate (200 mL). The extract was washed with water, saturated sodium hydrogen carbonate solution (NaHCO3, 100 mL×2) and aqueous sodium chloride solution, dried (anhydrous Na2SO4), and concentrated under reduced pressure. The residue was separated by column chromatography (10-20% ethyl acetate-hexane) to give 530 mg (49%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481537B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-7830b315d03c4eefa020a6b8692b6a16 |
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| Source note | uspto-grants-2013_07 |
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