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HRID 219567Erstellt: 25. Oktober 2026

Water → 5-benzyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylic acid

https://huagongshe.com/reaction/219567

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
EduktMethyl 5-benzyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylateHCID 68649205—
LösungsmittelEthanolHCID 702—
Produkt5-benzyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylic acidHCID 59604228—

Reaktionsschritte

Methyl 5-benzyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylate obtained in Step 1 as described above was dissolved in EtOH and NaOH (8.10 ml; 5 M; 40.48 mmol; 5 eq.) was added, the mixture was stirred overnight at room temperature. Water (30 mL) was added and the aqueous phase was washed with Et2O (2×30 mL). The aqueous layer was acidified to pH 2 with HCl 5 N and extracted with EtOAc (2×50 mL). The combined organics were washed with brine, dried over MgSO4 and concentrated under vacuum affording the title compound as a yellow oil. It was taken up in petroleum ether and it was sonicated. The suspension was filtered off, affording Intermediate 24 as a beige solid. 1H-NMR (DMSO-d6, 300 MHz) δ 13.43 (br s, 1H), 7.74-7.69 (m, 1H), 7.64-7.58 (m, 1H), 7.53-7.42 (m, 2H), 7.22-7.17 (m, 3H), 6.83-6.72 (m, 2H), 4.38 (s, 2H). LC/MS (Method B): 298.2 (M+H)+. HPLC (Method A) Rt 3.60 min (Purity: 92.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202856B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-ee0e489745374110b519ad620b700ca9
Quellennotizuspto-grants-2012_06