HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 23031297, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1H-Pyrrole-2-methanaminium, N,N,N-trimethyl-, iodide (1:1) | HCID 13975138 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23031297 | HCID 23031297 | 152.7% |
Reaction Steps
Subsequently, to a suspension of (pyrrol-2-yl)methyl trimethylammonium iodide (7.59 g, 28.52 mmol) obtained above in acetonitrile (60 ml) was added triphenylphosphine (8.98 g, 34.2 mmol) with stirring, and the resulting mixture was stirred at 80° C. for 6 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 (pyrrol-2-yl)methyl trimethylphosphonium iodide (12.33 g, yield: 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199150B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-69096e8bd7294c3bb13089ea8e4bb274 |
| Source note | uspto-grants-2007_04 |