Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754564Generated: October 28, 2026

2,2,2-Trifluoroethyl trifluoromethanesulfonate → HCID 86679809, compound

https://huagongshe.com/reaction/1754564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86679808HCID 86679808—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 86679809HCID 8667980973%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of N-(5-chloro-4-fluoro-2-iodophenyl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-4-carboxamide (1.26 g, 3.13 mmol) in 55 mL of anhydrous MeTHF heated to 65° C. are added potassium t-butoxide (421 mg, 3.76 mmol) and 2,2,2-trifluoroethyl trifluoromethanesulfonate (0.54 mL, 3.76 mmol). The reaction mixture is stirred for 2 hours at 65° C., and then cooled, poured into saturated aqueous NaHCO3 solution and extracted with EtOAc. The organic phase is washed with saturated aqueous NaCl solution, dried over Na2SO4 and concentrated to dryness. After purification by flash chromatography on silica (DCM/EtOAc: 100/0 to 95/5), 2.32 g of an orange-coloured solid are obtained (yield: 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169246B2
Source datasetuspto-grants-2015_10
ORD IDord-fb59ea5c5daf44cda5d080e11c659602
Source noteuspto-grants-2015_10