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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347543Erstellt: 25. Oktober 2026

Sodium Hydroxide → 1-(4-Fluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid

https://huagongshe.com/reaction/347543

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktMethyl 1-(4-fluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 21081722—
LösungsmittelMethanolHCID 887—
Produkt1-(4-Fluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acidHCID 1689668370,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of methyl 1-(4-fluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carboxylate (2.4 g, 9.2 mmol, 1.0 eq) in MeOH (25 ml) was treated with 5 N aqueous sodium hydroxide (4.6 mL, 24 mmol, 2.6 eq) at room temperature and the reaction mixture was stirred for 15 h. The reaction mixture was concentrated in vacuo, diluted with water and the solution was extracted with ethyl acetate (discarding the organic fraction). The aqueous fraction was cooled to 0° C. and acidified with concentrated HCl. The resulting solid was filtered, washed with water and the solid dried in vacuo to afford the product (1.6 g, 70%) which was sufficiently pure to use in the subsequent step without further purification. 1H NMR (DMSO-d6) δ 8.44–8.39 (m, 2H), 7.46–7.42 (m, 2H), 7.24–7.18 (m, 2H), 6.78 (d, 1H, J=6.98 Hz), 5.31 (s, 2H); HRMS(ESI), calcd.: 248.0723, found: 248.0718.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173031B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-f0bf1cb336424f24ac8e4e0fa99e5073
Quellennotizuspto-grants-2007_02