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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430420Generated: October 26, 2026

Methanesulfonyl fluoride, trifluoro- → HCID 11066809, compound

https://huagongshe.com/reaction/430420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl fluoride, trifluoro-HCID 67631—
ReactantFluorene-9-ethanolHCID 10921761—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506815HCID 178506815—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 11066809HCID 11066809—

Reaction Steps

To a solution of 21.0 g 2-(9-fluorenyl)ethanol, in 495 mL toluene was added dropwise with stirring 40 mL of a 2.5M solution of n-butyllithium in hexane. The resulting solution of Li{flu-CH2—CH2—O} was cooled to below −25° C. Then, 16.7 g CF3SO2F was condensed into the reaction mixture. Tile temperature was allowed to rise to 25° C. and the reaction mixture was stirred for 6 h. Unreacted CF3SO2F was removed by pumping about 10 mL of liquid into a dry ice-cooled trap. To the solution of flu-CH2—CH2—OSO2CF3 thus obtained was added a solution of 0.1 mole indenyllithium in 100 mL diethyl ether. After stirring for 12 h, solvents were removed under vacuum and the residue recrystallized in air from boiling heptane. The yield of white microcrystalline solid, mp 79-80° C., was 8.9 g (29%). Spectroscopic and chemical analysis confirmed the identity of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323151B1
Source datasetuspto-grants-2001_11
ORD IDord-93afc58766274cefb9ab25adf77edb69
Source noteuspto-grants-2001_11