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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422937Generated: October 30, 2026

Triphenylphosphine → (1-Ethylpyrrol-2-yl)methyltriphenylphosphonium iodide

https://huagongshe.com/reaction/422937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(1-Ethylpyrrol-2-yl)methyltrimethylammonium iodideHCID 23031652—
SolventAcetonitrileHCID 6342—
Product(1-Ethylpyrrol-2-yl)methyltriphenylphosphonium iodideHCID 2303150281.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

Subsequently, to a suspension of (1-ethylpyrrol-2-yl)methyl trimethylammonium iodide (20 g, 68.0 mmol) obtained above in acetonitrile (200 ml) was added triphenylphosphine (22.0 g, 83.9 mmol), and the resulting mixture was stirred at 80° C. for 9 hours. After cooling, the reaction mixture was concentrated to about one-half of its initial volume, to which was added ethyl acetate (100 ml). The crystals precipitated were collected by filtration, washed with ethyl acetate and dried in vacuo to afford the title compound (27.5 g, yield: 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101650B2
Source datasetuspto-grants-2012_01
ORD IDord-010b5bb657134efeb7321e4798edafee
Source noteuspto-grants-2012_01