HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → [(4-Nitrophenyl)methyl](triphenyl)phosphanium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(4-Nitrophenyl)methyl](triphenyl)phosphanium bromide | HCID 197008 | 99% |
Reaction Steps
A mixture of 4-nitrobenzylbromide (25.0 g, 0.116 mol), triphenylphosphine (30.4 g, 0.116 mol) and chloroform (120 ml) was refluxed for 2 hours with stirring. The mixture was cooled to room temperature, diluted with THF (250 ml) and cooled in a freezer for 4 hours. The solid was collected and dried under vacuum to give p-nitrobenzyl triphenylphosphonium bromide (54.8 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05605726 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-d57f463516bf46f48c9121469464878e |
| Source note | uspto-grants-1997_02 |