HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2,2'-(1,3-Phenylene)bis[1,10-phenanthroline]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,3-Diacetylbenzene | HCID 23229 | — |
| Reactant | 8-Aminoquinoline-7-carboxaldehyde | HCID 11052098 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,2'-(1,3-Phenylene)bis[1,10-phenanthroline] | HCID 10670470 | 83% |
Reaction Steps
101 g of 8-amino-7-quinoline carboaldehyde was reacted with 45 g of 1,3-diacetylbenzene and 100 g of 85% potassium hydroxide in 1800 ml of ethanol for 10 hours while refluxing and a reactant was treated by a normal method to obtain 100 g of 1,3-di(1,10-phenanthroline-2-yl)benzene. 40.8 g of this 1,3-di(1,10-phenanthroline-2-yl)benzene was reacted with 400 ml of phenyl lithium (0.94 M cyclohexane-ether solution) in 750 ml of toluene for 2.5 hours while cooling with ice and a reactant was treated by a normal method. The obtained product was reacted with 118 g of nitrobenzene at 110° C. for 3 hours and a reactant was treated by a normal method to obtain 22.8 g of E-20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114529B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-ff052704ccb94db2b6875eb26902b4b5 |
| Source note | uspto-grants-2012_02 |