HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-{3-[3-(4-Fluorophenoxy)propoxy]phenyl}-ethyl triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-{3-[3-(4-Fluorophenoxy)propoxy]phenyl}-ethyl bromide | HCID 19755708 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-{3-[3-(4-Fluorophenoxy)propoxy]phenyl}-ethyl triphenylphosphonium bromide | HCID 86745008 | 50% |
Reaction Steps
A solution of 20 mmol of bromide (example 141) and 30 mmol of triphenyl phosphine in 60 ml of ethanol was refluxed 20 hours under nitrogen and then cooled and evaporated in vacuo. The residue was chromatographed on silica gel using first CHCl3 to elute starting material residues and then 5% CH3OH in CHCl3 to elute the product. Evaporation of pure fractions yielded the title compound as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05159097 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-234f14db61f24964b55ead5bb561f661 |
| Source note | uspto-grants-1992_10 |