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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 344567Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-Chloro-4,6-dimethoxypyrimidine

https://huagongshe.com/reaction/344567

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Edukt2-Amino-4,6-dimethoxypyrimidineHCID 118946—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
Produkt2-Chloro-4,6-dimethoxypyrimidineHCID 5152323—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1,260 ml of 36% hydrochloric acid were charged in a 5-l four-necked flask and then cooled to 0° C. After 180 g (1.16 moles) of 2-amino-4,6-dimethoxypyrimidine were added in small portions into the flask, the resulting mixture was stirred for about 1 hour until the reaction mixture changed into a syrupy form. After the reaction mixture was cooled to -15° C., 260 ml of 159 g (2.3 moles) of NaNO2 in H2O were added dropwise over about 1 hour under vigorous stirring. After completion of the dropwise addition, the resulting mixture was stirred at -15° to -10° C. for additional 1 hour so that the reaction was brought to completion. While the reaction mixture was retained at -5° C., 1.5 l of a 30% aqueous solution of NaOH were charged dropwise so that the reaction mixture was neutralized to pH 7. By filtration under reduced pressure, a clay-like material of a purple color was collected. The target compound was extracted from the clay-like material using 3 l of ethyl acetate. Through the procedure of washing with water, drying over anhydrous sodium sulfate and removal of the solvent, 63 g of bluish crude crystals were obtained. They were crystallized further by silica get chromatography to obtain 60.8 g of white crystals (yield: 29.9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05053070
Quelldatensatzuspto-grants-1991_10
ORD IDord-a6cf9824225a4bec819a9d194fa5be81
Quellennotizuspto-grants-1991_10