HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodobenzene → 2-phenyl-2,3-dihydrofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-phenyl-2,3-dihydrofuran | HCID 10888052 | 58% |
Reaction Steps
Table 1, Entry 5. In the reaction tube were mixed iodobenzene (0.102 g, 0.5 mmol), dihydrofuran (0.350 g, 5.0 mmol), palladium acetate (0.00281 g, 0.0125 mmol), potassium acetate (0.147 g,1.5 mmol), n-Bu4NCl (0.139 g, 0.5 mmol), triphenylphosphine (0.00328 g, 0.0125 mmol) and 1.0 ml DMF.under nitrogen. The contents of the flask were irradiated for 6.00 min with an effect of 60 W. After cooling, the product mixture was poured into 25 ml water and was extracted three times with 25 ml DCM. The combined extracts were washed with 25 ml water and concentrated to an oil. The crude product was purified by column chromatography on silica gel using pentaneldiethyl ether (19/1) as the eluent. The yield was 58% (yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136157 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-ecee3b0fcc474c9593d591808a029019 |
| Source note | uspto-grants-2000_10 |