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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355166Generated: October 30, 2026

Triphenylphosphine → (Cyclopentylmethyl)triphenylphosphonium iodide

https://huagongshe.com/reaction/1355166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(Iodomethyl)cyclopentaneHCID 2762531—
SolventAcetonitrileHCID 6342—
Product(Cyclopentylmethyl)triphenylphosphonium iodideHCID 2231531992%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of iodomethylcyclopentane (129.38 g, 0.616 mol) and triphenylphosphine (161.54 g, 0.616 mol) in acetonitrile (308 mL) was heated under reflux for 9 d. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo to provide a solid. The solid was triturated with diethyl ether and then filtered. The solid was washed well with diethyl ether until the washings showed the absence of iodomethylcyclopentane and triphenylphosphine by thin layer chromatography. The resulting solid was allowed to air dry to afford cyclopentylmethyl triphenylphosphonium iodide (266.92 g, 92%) as a light yellow solid: mp 195–198° C.; FAB-HRMS m/e calcd for C24H26P (M+H)+ 345.1772, found 345.1784.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223868B2
Source datasetuspto-grants-2007_05
ORD IDord-b3869714a2474207bee05c0c9ce41bce
Source noteuspto-grants-2007_05