HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947110Generated: October 26, 2026
Phosphorus oxychloride → Ethyl 4-chloro-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate
https://huagongshe.com/reaction/1947110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-Butyltriethylammoniumchloride | HCID 10888803 | — |
| Reactant | Ethyl 2,4-dihydroxy-6-methylpyridine-3-carboxylate | HCID 54676534 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 4-chloro-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 57859986 | 44% |
Reaction Steps
A mixture of ethyl 4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate (3.00 g, 15.2 mmol), phosphorus oxychloride (7.75 mL), n-butyltriethylammonium chloride (13.8 g, 60.8 mmol) and acetonitrile (60 mL) was stirred at 40° C. for 30 min and under refluxing conditions for 30 min. After cooling, the reaction mixture was concentrated under reduced pressure, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was washed with ethyl acetate-hexane mixed solution, and dried under reduced pressure to give the title compound (1.45 g, 44%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399449B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-68ae94e440ca4b78a11f49d01d72fc47 |
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| Source note | uspto-grants-2013_03 |
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