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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408858Generated: November 3, 2026

1-Bromo-3-fluorobenzene → ((S)-1-benzylpyrrolidin-3-yl)-(3-fluorophenyl)amine

https://huagongshe.com/reaction/2408858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
Reactant(3S)-(+)-1-Benzyl-3-aminopyrrolidineHCID 1519353—
ReactantSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
Product((S)-1-benzylpyrrolidin-3-yl)-(3-fluorophenyl)amineHCID 2908090888.8%

Reaction Steps

A toluene solution containing 2.2 g of (S)-1-benzylpyrrolidin-3-ylamine (12.5 mmol), 2.2 g of 3-bromofluorobenzene (12.5 mmol), 0.31 g of 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP, 0.51 mmol), 0.14 g of bis(dibenzylideneacetone)palladium (Pd(dba)2, 0.22 mmol), and 1.3 g of sodium tert-butoxide (13.2 mmol) was heated under reflux under a nitrogen atmosphere for 3 hours. The reaction solution was filtered to remove insoluble matter, and ethyl acetate and water were added to the filtrate to separate the solution into layers. The organic layer was washed with water, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=20:1→1:1). The eluent solvent was distilled off under reduced pressure to thereby obtain 3.0 g of oily colorless ((S)-1-benzylpyrrolidin-3-yl)-(3-fluorophenyl)amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815871B2
Source datasetuspto-grants-2014_08
ORD IDord-0978ed8ec1ee493baed491ba90525860
Source noteuspto-grants-2014_08