HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552842Generated: November 1, 2026
Hydrochloric Acid → HCID 59214340, compound
https://huagongshe.com/reaction/552842
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isobutyl iodide | HCID 10556 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | Methyl 2-oxo-1,2-dihydropyridine-4-carboxylate | HCID 280755 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59214340 | HCID 59214340 | — |
Reaction Steps
LiH (78 mg) was suspended in DMF (5 ml), and a suspension of methyl-2-oxo-1,2-dihydropyridine-4-carboxylate (500 mg) in DMF (5 ml) was added dropwise thereto at room temperature. The suspension was stirred as it was, and a solution of 1-iodo-2-methylpropane (506 μl) in DMF (5 ml) was added dropwise thereto over 10 min, followed by stirring at 50° C. for 15 hours. To the reaction solution was added 1M HCl at 0° C., followed by extraction with EtOAc, and the organic layer was washed with saturated brine, dried over anhydrous MgSO4, and filtered, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (n-hexane:EtOAc=90:10 to 50:50) to obtain methyl-1-isobutyl-2-oxo-1,2-dihydropyridine-4-carboxylate (440 mg) as white powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951825B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d07f8556e3f54dcfa47f49aeb45f1fed |
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| Source note | uspto-grants-2011_05 |
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