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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389159Generated: October 30, 2026

Trifluoroacetic acid → HCID 58243781, compound

https://huagongshe.com/reaction/389159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58243583HCID 58243583—
ReactantHCID 58243616HCID 58243616—
SolventTolueneHCID 1140—
ProductHCID 58243781HCID 5824378128.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-methyl-2-(2,4,6-trifluorophenoxy)propanohydrazide (500 mg) and trifluoroacetic acid (0.08 ml) were added to a solution of ethyl 1-[(ethylimino)(methylsulfanyl)methyl]piperidine-4-carboxylate (600 mg) in toluene (10 ml), followed by stirring at 120° C. for 8 hours. An aqueous saturated sodium hydrogen carbonate solution was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate and the solvent was then evaporated. The resulting residue was purified by silica gel column chromatography (using basic silica:hexane:ethyl acetate=100:0 to 50:50 to 0:100) to obtain ethyl 1-{4-ethyl-5-[1-methyl-1-(2,4,6-trifluorophenoxy)ethyl]-4H-1,2,4-triazol-3-yl}piperidine-4-carboxylate (254 mg), as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-8c818e0387ab437bbd6263218148b9fd
Source noteuspto-grants-2013_02