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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80410Generated: October 29, 2026

Potassium Carbonate → 2-Methyl-4-trifluoromethylsulfanyl-2-(2-trifluoromethylsulfanyl-ethanesulfonyl)-butyronitrile

https://huagongshe.com/reaction/80410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Trifluoromethylthio)ethyl TrifluoromethanesulfonateHCID 25242028—
Reactant(2-Trifluoromethylsulfanyl-ethanesulfonyl)-acetonitrileHCID 86673275—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Methyl-4-trifluoromethylsulfanyl-2-(2-trifluoromethylsulfanyl-ethanesulfonyl)-butyronitrileHCID 86673274—

Reaction Steps

A mixture of (2-trifluoromethylsulfanyl-ethanesulfonyl)-acetonitrile (190 mg, 0.81 mmol), trifluoro-methanesulfonic acid 2-trifluoromethylsulfanyl-ethyl ester (340 mg, 1.22 mmol) and K2CO3 (340 mg, 2.44 mmol) in 1,2-dimethoxyethane (10 mL) was stirred under nitrogen at room temperature overnight. The reaction mixture was diluted with H2O (40 mL) and extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with saturated aqueous NaCl solution, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (SiO2, gradient of EtOAc/cyclohexane) to afford compound II-26 (20 mg, 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846569B2
Source datasetuspto-grants-2014_09
ORD IDord-b9c21e2525bb471e8f7024d02c8f9b7d
Source noteuspto-grants-2014_09