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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510467Generated: November 4, 2026

Triethylamine → Ethyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1510467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantEthyl 4-hydroxy-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 54685351—
ProductEthyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 1161545167%

Reaction Steps

Triethyl amine (7.07 mL, 50.7 mmol) was added to a suspension of 4-hydroxy-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl ester (10.0 g, 50.7 mmol) and POCl3 (27.85 mL, 304.3 mmol). After stirring 16 hours, the reaction mixture was concentrated under reduced pressure. The resulting residue was poured onto ice, carefully neutralized with saturated K2CO3 solution, and diluted with EtOAc. The layers were separated and the aqueous phase further extracted with EtOAc. The combined organic extracts were dried (MgSO4) and concentrated under reduced pressure to yield 7.3 g (67%) clean desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211920B2
Source datasetuspto-grants-2012_07
ORD IDord-1f9714cb6b434b9fa4fa1d471bec5866
Source noteuspto-grants-2012_07