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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108803Generated: October 31, 2026

Perfluorooctanesulfonyl fluoride → (3S,4S)-1-benzyloxycarbonyl-3-bromomethyl-4-fluoropyrrolidine

https://huagongshe.com/reaction/2108803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluorooctanesulfonyl fluorideHCID 9388—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(3S,4R)-Benzyl 3-(bromomethyl)-4-hydroxypyrrolidine-1-carboxylateHCID 66704866—
SolventTolueneHCID 1140—
Product(3S,4S)-1-benzyloxycarbonyl-3-bromomethyl-4-fluoropyrrolidineHCID 66704843—

Reaction Conditions

Temperature2 °C

Reaction Steps

Process B: (3S,4R)-1-Benzyloxycarbonyl-3-bromomethyl-4-hydroxypyrrolidine (492 mg) was dissolved in toluene (1 mL). To this solution, 1,8-diazabicyclo[5.4.0]undec-7-ene (0.35 mL) was added and perfluoro-1-octanesulfonylfluoride (0.42 mL) was subsequently added dropwise while the mixture was chilled in an ice water bath. The reaction mixture was stirred at 2° C. for 30 min and then at room temperature for 5 hours. Subsequently, the mixture was poured on a silica gel pad and was eluted with ethyl acetate (80 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)-1-benzyloxycarbonyl-3-bromomethyl-4-fluoropyrrolidine as a milky white syrup (421 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514451B2
Source datasetuspto-grants-2009_04
ORD IDord-d9709360187746f1875ba57cc83e3e78
Source noteuspto-grants-2009_04