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HRID 336639Erstellt: 25. Oktober 2026

2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- → ethyl 6-hydroxy-2-methyl-4-oxo-1H-pyridine-3-carboxylate

https://huagongshe.com/reaction/336639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Butenoic acid, 3-amino-, ethyl ester, (2Z)-HCID 643756—
EduktBis(2,4,6-trichlorophenyl) propanedioateHCID 2783450—
LösungsmittelBromobenzeneHCID 7961—
LösungsmittelEthyl AcetateHCID 8857—
Produktethyl 6-hydroxy-2-methyl-4-oxo-1H-pyridine-3-carboxylateHCID 17847003986%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of malonic acid (20 g, 192 mmol), 2,4,6-trichlorophenol (72 g, 365 mmol), and phosphorus oxychloride (38 mL, 403.2 mmol) was stirred at reflux for 12 h. The reaction mixture was cooled to 70° C. and poured into ice water. The solid was collected by filtration, washed with water, and air-dried to give malonic acid bis-(2,4,6-trichloro-phenyl)ester (85 g, 95%). A solution of malonic acid bis-(2,4,6-trichloro-phenyl)ester (85 g, 183.6 mmol) and ethyl 3-aminocrotonate (26.1 g, 202 mmol) in bromobenzene (100 mL) was stirred at reflux for 50 min. The reaction mixture was cooled to 50° C. and diluted with EtOAc (260 mL). The solid was collected by filtration, washed with water, and air-dried, to give 4,6-dihydroxy-2-methyl nicotinic acid ethyl ester (31 g, 86%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889698B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-bf916b2056694b5d8b39f2d993f7264f
Quellennotizuspto-grants-2014_11