HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 68769064, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 68769027 | HCID 68769027 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68769064 | HCID 68769064 | — |
Reaction Steps
2-(2-Phenyl-benzofuran-5-yl)ethanol (11.18 g; 46.9 mmol) was dissolved in DCM (170 ml) and N-iodinesuccinimide (NIS; 11.31 g; 50.27 mmol) and triphenylphosphine (15.39 g; 52.67 mmol) was added under stirring. After keeping the reaction mixture at RT over night the reaction was extracted two times with 6% aqueous NaHCO3 solution and the organic layer was dried over Na2SO4. After filtering and removal of the solvent pure title compound was obtained after crystallization from methanol/DCM/cyclo-hexane. The mother liquor was collected and purified on silica gel (cyclohexane/ethylacetate 95/5 as mobile phase).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825260B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-4ba8080ee9b64b3093db95dc43daf49e |
| Source note | uspto-grants-2010_11 |