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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906934Generated: November 2, 2026

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

https://huagongshe.com/reaction/906934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyltriphenylphosphonium iodideHCID 638159—
Reactant(3R,4S)-1-Benzyl-4-(3,4-dichloro-phenyl)-pyrrolidine-3-carbaldehydeHCID 86627623—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(3S,4R)-1-Benzyl-3-(3,4-dichloro-phenyl)-4-vinyl-pyrrolidineHCID 6713147080%

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 (3R,4S)-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 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 (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-79b2ab09fbc2426d9d1f2100c72e9a72
Source noteuspto-grants-2011_09