HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2,6-Bis(trifluoromethyl)benzyltriphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,6-Bis(trifluoromethyl)benzyl bromide | HCID 11851363 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Bis(trifluoromethyl)benzyltriphenylphosphonium bromide | HCID 86632155 | — |
Reaction Steps
To a solution of 2,6-bis(trifluoromethyl)benzyl bromide (0.400 g, 1.30 mmol) in toluene (5 mL) was added triphenylphosphine (0.375 g, 1.43 mmol). The mixture was heated to reflux for 24 h. After cooling to room temperature, hexanes (10 mL) was added and the mixture was stirred for 1 h. The solid was collected by filtration and rinsed with hexanes to give 2,6-bis(trifluoromethyl)benzyltriphenylphosphonium bromide as a white solid. Yield (0.446 g, 60%): 1H NMR (400 MHz, DMSO-d6) δ 8.02 (d, J=8.0 Hz, 2H), 7.57-7.87 (m, 16H), 5.17 (d, J=15.2 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420863B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-385e751663e14244ba772cb0f320bae6 |
| Source note | uspto-grants-2013_04 |