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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604546Generated: October 30, 2026

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

https://huagongshe.com/reaction/604546

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 Conditions

Temperature80 °C

Reaction Steps

(1-Methylpyrrol-2-yl)methyltrimethylammonium iodide (55.3 g, 198 mmol) was suspended in acetonitrile (400 mL) and triphenylphosphine (62.2 g, 237 mmol) was added thereto, followed by stirring of the mixture at 80° C. for 10 hours. After cooling, the mixture was concentrated to about 1/2 under reduced pressure, ethyl acetate (200 mL) was added thereto, and the precipitated crystal was collected by filtration. The crystal was washed with ethyl acetate and dried under reduced pressure to obtain the title compound (77.1 g, yield: 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910617B2
Source datasetuspto-grants-2011_03
ORD IDord-306edc649297446a8c868c087c7aeb76
Source noteuspto-grants-2011_03