HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (1-Methylpyrrol-2-yl)methyltriphenylphosphonium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N,N,N-Trimethyl(1-methyl-1H-pyrrol-2-yl)methanaminium iodide | HCID 12346658 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (1-Methylpyrrol-2-yl)methyltriphenylphosphonium iodide | HCID 23031470 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101650B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-6a73504917bb4dbe8dabfd4650b9ded1 |
| Source note | uspto-grants-2012_01 |