HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-(2-Octyl-benzo[1,3]dioxol-5-yl)-2-octyloxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-bromo-2-(octyloxy)Pyridine | HCID 14439231 | — |
| Reactant | 2-Octyl-benzo[1,3]dioxole-5-boronic acid | HCID 19050313 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Octyl-benzo[1,3]dioxol-5-yl)-2-octyloxypyridine | HCID 19050287 | — |
Reaction Steps
5 mmol of 2-octyl-benzo[1,3]dioxole-5-boronic acid and 5 mmol of 5-bromo-2-octyloxypyridine are introduced into a mixture of 30 ml of toluene, 15 ml of ethanol and 15 ml of water. 0.05 mmol of tetrakis(triphenylphosphine)palladium(O) and 12 mmol of sodium carbonate are added, and the mixture is refluxed for 6 hours. The phases are separated, the aqueous phase is extracted with tert-butyl methyl ether, and the combined organic phases are dried by means of Na2SO4. For further purification, the substance is chromatographed on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05626791 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-ee4a009f4b65474ba52575dbfaade247 |
| Source note | uspto-grants-1997_05 |