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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906943Generated: November 2, 2026

Methyltriphenylphosphonium iodide → (3S,4R)-1-Benzyl-3-(3,4-difluoro-phenyl)-4-vinyl-pyrrolidine

https://huagongshe.com/reaction/906943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyltriphenylphosphonium iodideHCID 638159—
Reactant(3R,4S)-1-Benzyl-4-(3,4-difluoro-phenyl)-pyrrolidine-3-carbaldehydeHCID 86627625—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(3S,4R)-1-Benzyl-3-(3,4-difluoro-phenyl)-4-vinyl-pyrrolidineHCID 6713149562%

Reaction Steps

To a suspension of methyltriphenylphosphonium iodide (6.35 g, 15.6 mmol) in THF (60 mL) was added n-BuLi (1.6N in heptane, 7.4 mL, 0.0119 mol) dropwise at 0° C. and stirred for one hour. To this reaction mixture was added a solution of (3R,4S)-1-benzyl-4-(3,4-difluoro-phenyl)-pyrrolidine-3-carbaldehyde 2.77 g (9.2 mmol) in THF (15 mL) dropwise at 0° C. and stirred for another one hour. The reaction was quenched by aq. ammonium chloride solution and extracted with ethylacetate. The separated organic layer was dired on anhydrous sodium sulfate and concentrated in vaccuo. The residue was purified by silica gel column chromatography eluted by a mixture of heptane and ethyl acetate (7:3) yielding 1.7 g (62%) of the title compound as a light yellow oil ES-MS m/e: 300.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012998B2
Source datasetuspto-grants-2011_09
ORD IDord-17990f086b9a4bd7b462ddb99a84c0da
Source noteuspto-grants-2011_09