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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269412Generated: October 30, 2026

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

https://huagongshe.com/reaction/1269412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN,N,N-Trimethyl(1-methyl-1H-pyrrol-2-yl)methanaminium iodideHCID 12346658—
SolventAcetonitrileHCID 6342—
Product(1-Methylpyrrol-2-yl)methyltriphenylphosphonium iodideHCID 2303147081%

Reaction Steps

Subsequently, to a suspension of (1-methylpyrrol-2-yl)methyl trimethylammonium iodide (55.34 g, 197.5 mmol) obtained above in acetonitrile (400 ml) was added triphenylphosphine (62.20 g, 237.1 mmol) with stirring, and the resulting mixture was stirred at 80° C. for 10 hours. After cooling, the reaction mixture was concentrated to about one-half of its initial volume, to which was added ethyl acetate (200 ml). The crystals precipitated were collected by filtration, washed with ethyl acetate and dried in vacuo to afford the title compound (77.14 g, yield: 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199150B2
Source datasetuspto-grants-2007_04
ORD IDord-3c15498b3a3e458981610e92febdef5f
Source noteuspto-grants-2007_04