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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269417Generated: October 30, 2026

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

https://huagongshe.com/reaction/1269417

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 numberUS07199150B2
Source datasetuspto-grants-2007_04
ORD IDord-b9967febb5d444d7a61c67bb7f14ff50
Source noteuspto-grants-2007_04