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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562639Generated: October 29, 2026

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

https://huagongshe.com/reaction/562639

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 (1.00 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 numberUS08067396B2
Source datasetuspto-grants-2011_11
ORD IDord-1caf8e1db92c480f9e1ac405c40251c8
Source noteuspto-grants-2011_11