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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1255800Erstellt: 26. Oktober 2026

Sodium ethoxide → 5-Bromo-2-ethylpyrimidine-4-carboxylic acid

https://huagongshe.com/reaction/1255800

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ethoxideHCID 2723922—
EduktMucobromic AcidHCID 3033972—
EduktSodiumHCID 5360545—
EduktPropionimidamide hydrochlorideHCID 12301253—
LösungsmittelEthanolHCID 702—
Produkt5-Bromo-2-ethylpyrimidine-4-carboxylic acidHCID 6697770237%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

Sodium (356 mg, 15.5 mmol) was carefully added to ethanol (5.9 mL) to prepare sodium ethoxide solution in ethanol. The above freshly prepared ethanol solution (3.5 mL) was added to a stirred suspension of propionimidamide hydrochloride (1.05 g, 9.69 mmol). The mixture was warmed to 55° C., then the heating bath was removed and a solution of mucobromic acid (1 g, 3.87 mmol) in ethanol was added dropwise at a rate which maintained a constant temperature, followed by a further sodium ethoxide solution (2 mL). After cooling, the mixture was filtered and evaporated to a residue which was shaken vigorously with hydrochloric acid (2 M×2.4 mL). The brown precipitate was filtered off and washed with cold water, then freeze-dried to give 5-Bromo-2-ethylpyrimidine-4-carboxylic acid (330 mg, 37%) as a yellow solid. LCMS: 231 [M+1]+, 1H NMR (400 MHz, DMSO-d6): δ 1.25 (t, J=7.6 Hz, 3H), 2.88 (q, J=7.6 Hz, 2H), 9.05 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08461157B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-50672b3b031641a89651b56c4c1cebcc
Quellennotizuspto-grants-2013_06