HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422937Generated: October 30, 2026
Triphenylphosphine → (1-Ethylpyrrol-2-yl)methyltriphenylphosphonium iodide
https://huagongshe.com/reaction/422937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (1-Ethylpyrrol-2-yl)methyltrimethylammonium iodide | HCID 23031652 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (1-Ethylpyrrol-2-yl)methyltriphenylphosphonium iodide | HCID 23031502 | 81.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101650B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-010b5bb657134efeb7321e4798edafee |
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| Source note | uspto-grants-2012_01 |
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