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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660101Generated: October 31, 2026

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

https://huagongshe.com/reaction/660101

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 numberUS08084442B2
Source datasetuspto-grants-2011_12
ORD IDord-eb5add572dfd45ce871c0484e23348c1
Source noteuspto-grants-2011_12