HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Triphenylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | O-Terphenyl | HCID 6766 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Triphenylene | HCID 9170 | 35% |
Reaction Steps
2.87 mmol of the o-terphenyl derivative, 0.14 mmol of Pd(OAc)2 and 5.7 mmol of K2CO3 are heated in 7 ml of DMA at 135° C. for 24 hours under a nitrogen atmosphere. The reaction mixture is cooled, treated with 5 ml of water and extracted with dichloromethane. The organic phase is dried, the solvent is removed under reduced pressure and the residue is purified by means of a short silica gel column (dichloromethane). After column chromatography (dichloromethane/hexane, 2:1), the desired triphenylene derivative (IIa) is obtained in from 35 to 40% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455112B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-bed0d9afd4144f1387089f43035b718c |
| Source note | uspto-grants-2013_06 |