HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphonium hydrobromide → {5-Fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]benzyl}triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphonium hydrobromide | HCID 22178555 | — |
| Reactant | 5-Fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]benzyl alcohol | HCID 57864413 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | {5-Fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]benzyl}triphenylphosphonium bromide | HCID 86634291 | 82.5% |
Reaction Steps
1.7 g (5.41 mmol) of {5-fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]phenyl}methanol and 1.76 g (5.14 mmol) of triphenylphosphonium hydrobromide are heated under reflux in 20 ml of acetonitrile for three hours. A first product fraction is crystallized at −20° C. The mother liquor is concentrated, the residue is dissolved in dichloromethane, and a second fraction is crystallized with diethyl ether. A total of 2.71 g (76% yield) of the title compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998988B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-25124effb83040bf96eac9300a88a2d8 |
| Source note | uspto-grants-2011_08 |