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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219564Generated: October 27, 2026

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

https://huagongshe.com/reaction/219564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl 3-cyclopropyl-3-oxopropanoateHCID 262979—
Reactant1-Azido-2-fluorobenzeneHCID 11607924—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-cyclopropyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylateHCID 68649104—

Reaction Steps

DBU (2.99 ml; 20.06 mmol; 1.10 eq.) was dissolved in DMF (37.5 ml) and put under nitrogen atmosphere. 3-Cyclopropyl-3-oxo-propionic acid ethyl ester (Betapharma, 3.132 g; 20.06 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, (2.5 g; 18.23 mmol; 1 eq.) in DMF (5 mL) was added dropwise to the solution at room temperature. Water (50 mL) was added to the cooled reaction mixture and the aqueous layer was extracted with EtOAc (3×50 mL). Combined organics were washed with water and 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. LC/MS (Method B): 276.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202856B2
Source datasetuspto-grants-2012_06
ORD IDord-59ffb5b717d145edbe0ffa8943f7b38d
Source noteuspto-grants-2012_06