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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108808Generated: October 31, 2026

Perfluorooctanesulfonyl fluoride → HCID 66704853, compound

https://huagongshe.com/reaction/2108808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluorooctanesulfonyl fluorideHCID 9388—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 66704846HCID 66704846—
SolventTolueneHCID 1140—
ProductHCID 66704853HCID 66704853—

Reaction Conditions

Temperature2 °C

Reaction Steps

Process B: (3S,4R)-3-Bromomethyl-1-tert-butoxycarbonyl-4-hydroxypyrrolidine (561 mg) was dissolved in toluene (20 mL). To this solution, 1,8-diazabicyclo[5.4.0]undec-7-ene (0.50 mL) was added and perfluoro-1-octanesulfonylfluoride (0.93 mL) was then added dropwise while the mixture was chilled in an ice water bath. After stirred at 2° C. for 1 hour, the reaction mixture was poured on a silica gel pad and was eluted with ethyl acetate (100 mL). The eluate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluant: hexane: ethyl acetate=2:1) to give (3S,4S)-3-bromomethyl-1-tert-butoxycarbonyl-4-fluoropyrrolidine as a yellow oil (447 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514451B2
Source datasetuspto-grants-2009_04
ORD IDord-0d6dc8abee5a46a9bc98d451e9ec3184
Source noteuspto-grants-2009_04