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HRID 30633Erstellt: 23. Oktober 2026

Hydrochloric Acid → (2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acid

https://huagongshe.com/de/reaction/30633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethyl phosphonoacetateHCID 13345—
EduktSodium hydrideHCID 24758—
Edukt4-(4-fluorophenyl)-4H-1,2,4-triazole-3-carbaldehydeHCID 83877613—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acidHCID 6920920877,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 4-(4-fluorophenyl)-4H-1,2,4-triazole-3-carbaldehyde (3.83 g), ethyl diethylphosphonoacetate (5.60 g), sodium hydride (60% in oil, 0.88 g) and tetrahydrofuran (130 ml) was stirred at 0° C. for 1 hr. The reaction mixture was poured into an aqueous dilute hydrochloric acid solution and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was dissolved in a 6N aqueous hydrochloric acid solution (100 ml) and stirred for 2 hrs. with heating under reflux. Disodium hydrogen phosphate was added to neutralize the reaction mixture. The precipitated solids were collected by filtration, washed with water and dried to give (2E)-3-[4-(4-fluorophenyl)-4H-1,2,4-triazol-3-yl]acrylic acid (3.60 g, yield 76%) as pale-yellow crystals. melting point: 226-229° C. (recrystallized from ethyl acetate-hexane).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423159B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-f587e4f7f1cf4ddc8ddbbf4804b567ee
Quellennotizuspto-grants-2008_09