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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198027Generated: October 26, 2026

1-Bromo-3,5-bis(trifluoromethyl)benzene → (3S)-1-[3,5-bis(trifluoromethyl)phenyl]pyrrolidin-3-ol

https://huagongshe.com/reaction/2198027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3,5-bis(trifluoromethyl)benzeneHCID 67602—
ReactantBinap, (A+-)-HCID 634876—
Reactant(S)-3-Hydroxypyrrolidine hydrochlorideHCID 22309122—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(3S)-1-[3,5-bis(trifluoromethyl)phenyl]pyrrolidin-3-olHCID 4694168228%

Reaction Steps

A solution of 3,5-bis(trifluoromethyl)phenyl bromide (44.0 g), (S)-3-hydroxypyrrolidine hydrochloride (17.8 g), tris(dibenzylideneacetone)dipalladium(0) (5.88 g), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (8.00 g) and sodium tert-butoxide (36.0 g) in toluene (280 ml) was refluxed with stirring under an argon gas atmosphere for 16 hr. After cooling to room temperature, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate 20:1-2:1) to give the title compound (12.0 g, yield 28%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338622B2
Source datasetuspto-grants-2012_12
ORD IDord-e645636b00b045c4adfdb98b6337d8c4
Source noteuspto-grants-2012_12