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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219565Generated: October 30, 2026

Water → Ethyl 1-(2-fluorophenyl)-5-(tetra hydrofuran-2-yl)-1H-1,2,3-triazole-4-carboxylate

https://huagongshe.com/reaction/219565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Azido-2-fluorobenzeneHCID 11607924—
ReactantEthyl 3-oxo-3-(oxolan-2-yl)propanoateHCID 22831882—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 1-(2-fluorophenyl)-5-(tetra hydrofuran-2-yl)-1H-1,2,3-triazole-4-carboxylateHCID 68649129—

Reaction Conditions

Temperature70 °C

Reaction Steps

Potassium carbonate (2.419 g; 17.50 mmol; 2 eq.) was dissolved in DMSO (18 ml) and put under nitrogen atmosphere. 1-Azido-2-fluorobenzene, prepared according to Platz, M. S. et al. J. Org. Chem. 1989, 54, 5938-5945, (1.2 g; 8.75 mmol; 1 eq.) was dissolved in 10 mL of DMSO and ethyl 3-(tetrahydrofuran-2-yl)-3-oxopropanoate (Pharmacore, 1.793 mg; 9.63 mmol; 1.10 eq.) was added. This solution was added dropwise to the potassium carbonate solution at room temperature. The mixture was stirred at 70° C. for 3 hours. Water (30 mL) was added to the mixture and it was extracted with EtOAc (2×40 mL). Organics were washed with brine, dried over MgSO4 and concentrated under vacuum affording the title compound as a brown oil. It was used in the next step without further purification. HPLC (Method A) Rt 4.14 min (Purity: 86.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202856B2
Source datasetuspto-grants-2012_06
ORD IDord-4297ff5b96fd428f97dff354b5c6ac86
Source noteuspto-grants-2012_06