HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dimethylethylenediamine → 2-(N,N-diphenylamino)-7-bromo-9,9-dimethylfluorene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2-Bromo-7-iodo-9,9-dimethyl-9H-fluorene | HCID 45382179 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(N,N-diphenylamino)-7-bromo-9,9-dimethylfluorene | HCID 58729745 | 69.9% |
Reaction Steps
Charged under Ar atmosphere were 2-bromo-7-iodo-9,9-dimethylfluorene 20.0 g, diphenylamine 8.46 g, copper iodide 0.476 g, N,N′-dimethylethylene-diamine 0.441 g, sodium t-butoxide 7.21 g and xylene 50 ml, and the mixture was refluxed for 24 hours under heating. After cooled down to room temperature, the mixture was extracted with toluene, and the insoluble matter was filtered. The filtrate was concentrated, and then the concentrate was refined by silica gel chromatography to obtain 15.4 g of a yellow solid matter of 2-(N,N-diphenylamino)-7-bromo-9,9-dimethylfluorene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425654B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-9fd63b03482f4e93a36ae9d35def82bf |
| Source note | uspto-grants-2008_09 |