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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15903Generated: October 27, 2026

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

https://huagongshe.com/reaction/15903

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

Triethylamine (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 numberUS07732616B2
Source datasetuspto-grants-2010_06
ORD IDord-ba7c21b737a34f55b00df87c3e004916
Source noteuspto-grants-2010_06