HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde, 4-(diphenylamino)- → 1H-Benz[f]indene-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1H-Benz[f]indene-1,3(2H)-dione | HCID 607233 | — |
Reaction Steps
Benz[f]indane-1,3-dione was synthesized according to J. Med. Chem., Vol. 16, paragraphs 1334 to 1339 (1973), and 2 g of this sample and 3.1 g of 4-(N,N-diphenylamino)benzaldehyde were heated with stirring in 20 ml of ethanol under reflux for 6 hours. After cooling to room temperature, the obtained crystal was separated by filtration, washed and recrystallized from chloroform-acetonitrile to obtain 4.3 g of Compound (1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08847208B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-3b7e7a14fc614c7697de423d0ee960fc |
| Source note | uspto-grants-2014_09 |