HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 4-Selenophen-2-ylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Iodoselenophene | HCID 142183 | — |
| Reactant | (2-Hydroxyphenyl)boronic acid | HCID 2773454 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 4-Selenophen-2-ylphenol | HCID 12612806 | — |
Reaction Steps
A mixture of 27.9 g (0.11 mol) of 2-iodoselenophene, 15.0 g (0.11 mol) of 2-hydroxyphenylboronic acid, 6.8 g (5.88 mmol) of tetrakis(triphenylphosphine)palladium(0) and 235 ml of 2 N sodium carbonate soln. in 600 ml of toluene/ethanol (1:1) is heated under reflux for 19 h. The mixture is diluted with MTBE and washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:MTBE=4:1→1:1). Further purification is carried out by digestion in cold n-heptane; 4-selenophen-2-ylphenol is obtained as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304036B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-0758f29e362d49169dbb883bb272b792 |
| Source note | uspto-grants-2012_11 |