HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphonium hydrobromide → Triphenyl[2-(4'-trifluoromethylbiphenyl-4-ylmethoxy)benzyl]phosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphonium hydrobromide | HCID 22178555 | — |
| Reactant | HCID 57864370 | HCID 57864370 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Triphenyl[2-(4'-trifluoromethylbiphenyl-4-ylmethoxy)benzyl]phosphonium bromide | HCID 86634287 | 96.7% |
Reaction Steps
A solution of 11.7 g (32.65 mmol) of [2-(4′-trifluoromethylbiphenyl-4-ylmethoxy)phenyl]methanol in 100 ml of acetonitrile is mixed with 10.64 g (31.02 mmol) of triphenylphosphonium hydrobromide and heated under reflux for 3 hours. The reaction solution is then evaporated to dryness, and the resulting oil is taken up and triturated in diethyl ether. The product crystallizes as a white solid. After filtration, the solid is dried in a drying oven at 50° C. overnight. 20.5 g (30 mmol, 92% yield) of crystalline product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609727B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-8f01b154268846469fed92037cc8afbc |
| Source note | uspto-grants-2013_12 |