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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219569Generated: October 30, 2026

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

https://huagongshe.com/reaction/219569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl isobutyrylacetateHCID 81583—
Reactant1-Azido-2-fluorobenzeneHCID 11607924—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(2-fluorophenyl)-5-isopropyl-1H-1,2,3-triazole-4-carboxylateHCID 68649348—

Reaction Steps

DBU (3.6 ml; 24.07 mmol; 1.10 eq.) was dissolved in DMF (45 ml) and put under nitrogen atmosphere. Ethyl isobutyrylacetate (Aldrich, 3.807 g; 24.07 mmol; 1.10 eq.) was added to the mixture and it was stirred for 15 min. Then a solution of 1-azido-2-fluorobenzene, prepared according to Platz, M. S. et al. J. Org. Chem. 1989, 54, 5938-5945, (3 g; 21.858 mmol; 1 eq.) in DMF (10 mL) was added dropwise to the solution at room temperature. The reaction mixture was stirred at 70° C. for 5 hours. Water (80 mL) was added to the reaction mixture. The aqueous layer was extracted with EtOAc (2×100 mL). Combined organics were washed with HCl 0.1N, brine, dried over MgSO4 and concentrated under vacuum giving the title compound as a brown oil. It was used in the next step without further purification. LC/MS (Method B): 278.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202856B2
Source datasetuspto-grants-2012_06
ORD IDord-b71d95016474453e8541cb1c85129c48
Source noteuspto-grants-2012_06