HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430420Generated: October 26, 2026
Methanesulfonyl fluoride, trifluoro- → HCID 11066809, compound
https://huagongshe.com/reaction/430420
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl fluoride, trifluoro- | HCID 67631 | — |
| Reactant | Fluorene-9-ethanol | HCID 10921761 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506815 | HCID 178506815 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 11066809 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323151B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-93afc58766274cefb9ab25adf77edb69 |
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| Source note | uspto-grants-2001_11 |
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