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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Ethyl isobutyrylacetate | HCID 81583 | — |
| Reactant | 1-Azido-2-fluorobenzene | HCID 11607924 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-(2-fluorophenyl)-5-isopropyl-1H-1,2,3-triazole-4-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08202856B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-b71d95016474453e8541cb1c85129c48 |
|---|
| Source note | uspto-grants-2012_06 |
|---|