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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Ethyl 3-cyclopropyl-3-oxopropanoate | HCID 262979 | — |
| Reactant | 1-Azido-2-fluorobenzene | HCID 11607924 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 5-cyclopropyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202856B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-59ffb5b717d145edbe0ffa8943f7b38d |
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| Source note | uspto-grants-2012_06 |
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