HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → 2-Phenylindeno[1,2,3-de]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | 1-Aminofluoren-9-one | HCID 80664 | — |
| Reactant | CID 3610038 | HCID 3610038 | — |
| Product | 2-Phenylindeno[1,2,3-de]quinoline | HCID 59621476 | 45% |
Reaction Steps
In a round-bottomed flask, 9.0 mmol of acetophenone, 3.0 mmol of 1-amino-9-fluorenone (manufactured by Aldrich), and 1.5 mmol of diphenyl phosphate were placed, and the resultant mixture was irradiated with microwave (2,450 MHz) for 10 minutes under argon atmosphere. The reaction solution was cooled to room temperature, concentrated, and then separated and purified by silica gel column chromatography (eluant: dichloromethane and methanol), to give 2-phenylindeno[1,2,3-de]quinoline. The isolation yield was 45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08136974B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-dc1332d986424a7fa61f074dab5a0fcd |
| Source note | uspto-grants-2012_03 |