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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906920Generated: October 31, 2026

Methyltriphenylphosphonium iodide → (3SR,4RS)-1-Benzyl-3-(3.4-dichloro-phenyl)-4-vinyl-pyrrolidine

https://huagongshe.com/reaction/906920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyltriphenylphosphonium iodideHCID 638159—
Reactant(3RS,4SR)-1-Benzyl-4-(3,4-dichloro-phenyl)-pyrrolidine-3-carbaldehydeHCID 86627621—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(3SR,4RS)-1-Benzyl-3-(3.4-dichloro-phenyl)-4-vinyl-pyrrolidineHCID 6713147680%

Reaction Steps

To a suspension of methyltriphenylphosphonium iodide (5.53 g, 0.0136 mol) in THF (50 mL) was added n-BuLi (1.6N in heptane, 6.5 mL, 0.0104 mol) dropwise at 0° C. and stirred for one hour. To this reaction mixture was added a solution of (3RS,4SR)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidine-3-carbaldehyde 2.68 g (0.008 mol) 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 dried 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 (4: 1) yielding 2.12 g (80%) of the title compound as a light yellow oil. ES-MS m/e: 332.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012998B2
Source datasetuspto-grants-2011_09
ORD IDord-e35a1f3f1fad402daa5f9945a4f842cd
Source noteuspto-grants-2011_09