HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → ethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (2-Fluorobenzyl)hydrazine | HCID 10374537 | — |
| Reactant | Ethyl 3-cyano-2-oxopropanoate | HCID 11309560 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | ethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate | HCID 11391384 | — |
Reaction Steps
111.75 g (75 ml, 0.98 mol) of trifluoroacetic acid are added to 100.00 g (0.613 mol) of the sodium salt of ethyl cyanopyruvate (prepared in analogy to Borsche and Manteuffel, Liebigs Ann. 1934, 512, 97) while stirring efficiently in 2.5 l of dioxane at room temperature under argon, and the mixture is stirred for 10 min, during which most of the precursor dissolves. Then 85.93 g (0.613 mol) of 2-fluorobenzyl-hydrazine are added, and the mixture is boiled overnight. After cooling, the sodium trifluoroacetate crystals which have separated out are filtered off with suction and washed with dioxane, and the remaining crude solution is reacted further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091198B1 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-347c075934a74b70a106dd279acbdf62 |
| Source note | uspto-grants-2006_08 |