HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromocyclopentane → Cyclopentyltriphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Cyclopentyltriphenylphosphonium bromide | HCID 2735896 | — |
Reaction Steps
Bromocyclopentane and triphenylphosphine are directly heated to 110° C. for 6 hrs in the absence of a solvent, and part of the unreacted raw material is dissolved in toluene, to obtain cyclopentyl triphenylphosphonium bromide. The resulting cyclopentyl triphenylphosphonium bromide is reacted with potassium tert-butoxide in the solvent tetrahydrofuran at 0° C. to generate the corresponding Ylide reagent, which undergoes Witting reaction with
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428693B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-b7451582eec04e62aa322dc410f98d95 |
| Source note | uspto-grants-2016_08 |