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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391015Erstellt: 23. Oktober 2026

Acetamidine monohydrochloride → 5-Bromo-2-methylpyrimidine-4-carboxylic acid

https://huagongshe.com/de/reaction/391015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetamidine monohydrochlorideHCID 67170—
EduktSodium ethoxideHCID 2723922—
EduktMucobromic AcidHCID 3033972—
LösungsmittelEthanolHCID 702—
Produkt5-Bromo-2-methylpyrimidine-4-carboxylic acidHCID 25621025,4%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of acetamidine hydrochloride (6.0 g) in ethanol (20 mL) was added sodium ethoxide (20 mL of a 21% solution in ethanol) and the reaction mixture was heated at 50° C. and mucobromic acid (6.82 g) in ethanol (10 mL) was added. After stirring at 50° C. for 1 h, a further portion of sodium ethoxide (10 mL of a 21% solution in ethanol) was added and the mixture was stirred at room temperature for 16 h. The mixture was then filtered and the filtrate reduced in vacuo. The residue was then treated with 2 M aqueous hydrochloric acid (30 mL) and stirred vigorously for 30 minutes. The resulting solid was filtered, washed with water and air dried to give 5-bromo-2-methyl-pyrimidine-4-carboxylic acid (1.46 g). This was then heated at 175° C. for 16 h. After cooling to room temperature the mixture was purified by Kugelrohr distillation to give 5-bromo-2-methyl-pyrimidine as a white solid (746 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383620B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-9cbfc31e361648e0a7a4ffb10d1c6fd4
Quellennotizuspto-grants-2013_02