HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → ((4'-Chlorobiphenyl-2-yl)methyl)triphenylphosphonium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4'-Chloro-2-(iodomethyl)biphenyl | HCID 67054293 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | ((4'-Chlorobiphenyl-2-yl)methyl)triphenylphosphonium iodide | HCID 86667196 | 93% |
Reaction Steps
To a solution of 4′-chloro-2-(iodomethyl)biphenyl in toluene (11 mL), triphenylphosphine (1.20 g, 4.57 mmol) was added. The result mixture was refluxed overnight, allowed to cool to room temperature and filtered. The solid was washed with ether and dried under vacuum to afford ((4′-Chlorobiphenyl-2-yl)methyl)triphenylphosphonium iodide (2.50 g, 93%): 1H NMR (400 MHz, chloroform-d) δ ppm 6.35-8.06 (m, 23 H), 5.12-5.63 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809352B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-08d64b8a1aa845e3ad194082dcb816ee |
| Source note | uspto-grants-2014_08 |