HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (2-Fluoro-5-nitrobenzyl)(triphenyl)phosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(Bromomethyl)-1-fluoro-4-nitrobenzene | HCID 10353967 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2-Fluoro-5-nitrobenzyl)(triphenyl)phosphonium bromide | HCID 86643536 | — |
Reaction Steps
20 g (85.5 mmol) of the compound from Example 26A are dissolved in 250 ml of anhydrous toluene, and 22.4 g (85.5 mmol) of triphenylphosphine are added. The solution is heated under reflux for 16 h, resulting in the formation of a precipitate. The mixture is allowed to cool, and the precipitate is filtered off. After washing with diethyl ether, the precipitate is dried under reduced pressure. This gives 39 g (92% of theory) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846934B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-26f40b40097c47ada2414ad639ecf279 |
| Source note | uspto-grants-2014_09 |