HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 9-Phenanthren-3-ylanthracene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | 6-Anthracen-9-ylphenanthrene-9-carboxylic acid | HCID 59629491 | — |
| Catalyst | HCID 178505374 | HCID 178505374 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Product | 9-Phenanthren-3-ylanthracene | HCID 59629500 | — |
Reaction Steps
40 g (94 mmol) of 6-anthracen-9-ylphenanthrene-9-carboxylic acid are suspended in 250 ml of quinoline, the suspension is saturated with N2, 11.8 g (38 mmol) of copper chromite are added, and the mixture is heated at the boil for eight hours. The mixture is subsequently poured into 1 l of MeOH/water, and the black solid is filtered off with suction, washed with MeOH and subjected to Soxhlet extraction with CHCl3. Removal of the solvent leaves a greyish solid, which is recrystallised twice from dioxane. The yield is 30.6 g (92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993123B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-fc400d9c518b466e9f83d4d1a64dc280 |
| Source note | uspto-grants-2015_03 |