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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1251356Erstellt: 27. Oktober 2026

Diethyl (ethoxymethylene)malonate → Ethyl 4-hydroxy-2-methylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/1251356

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl (ethoxymethylene)malonateHCID 6871—
EduktEthanimidamide, acetate (1:1)HCID 160356—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 4-hydroxy-2-methylpyrimidine-5-carboxylateHCID 29375046%

Reaktionsschritte

Acetamidine acetate (37.21 g, 0.31 mole) and diethyl ethoxymethylenemalonate (63 mL, 0.31 mole) were refluxed for 4 h in ethanol (60 mL). The reaction mixture was allowed to cool for 15 minutes, then acetamidine acetate (37.21 g, 0.31 mole) was added. The reaction mixture was refluxed for 22 hours, allowed to cool to room temperature, and diluted with water (200 mL) and dichloromethane (200 mL). The aqueous layer was extracted with 10% isopropanol/dichloromethane (2×200 mL). The combined organic extracts were washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered and the solvent was removed. The residue was recrystallized from chloroform/hexanes in two crops to afford the title compound (24.92 g) in 46% yield as yellowish crystals. Rf=0.27 (silica gel, 10% isopropanol in dichloromethane); m.p. 187 to 188° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06342504B1
Quelldatensatzuspto-grants-2002_01
ORD IDord-2d7c93ac1a45444c992a3723849be3da
Quellennotizuspto-grants-2002_01