HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1,10-Phenanthroline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 8-Aminoquinoline-7-carboxaldehyde | HCID 11052098 | — |
| Product | 1,10-Phenanthroline | HCID 1318 | — |
Reaction Steps
4.0 g of propellane, 3.3 g of aluminium chloride and 2.0 ml of acetyl chloride were added to 200 ml of 1,2-dichloroethane, and reaction carried out for 1.5 hours at room temperature and then for 6 hours at 60° C. By treatment in the normal way, 3.26 g of the triacetyl-propellane was obtained. 1.41 g of this triacetyl derivative was reacted with 1.50 g of 8-amino-7-quinolinecarbaldehyde and 1.5 g of potassium hydroxide in dioxane at 60° C. and, by treatment in the normal way, Phen-5 (1.32 g) shown below was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07318966B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-37e63e4f03634a108331c3a39a2c4f4a |
| Source note | uspto-grants-2008_01 |