HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acenaphthenequinone → 7,9-Diphenyl-8H-cyclopenta[a]acenaphthylen-8-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acenaphthenequinone | HCID 6724 | — |
| Reactant | 1,3-Diphenyl-2-propanone | HCID 7593 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7,9-Diphenyl-8H-cyclopenta[a]acenaphthylen-8-one | HCID 267145 | 71.3% |
Reaction Steps
An amount of 5.9 g (32.4 mmol) of acenaphthenequinone and 7.5 g (35.7 mmol) of 1,3-diphenyl-2-propanone were suspended in 150 ml of ethanol and a solution of 2 g of potassium hydroxide in ethanol was added. After the mixture was heated to the reflux temperature, the same amount of the solution of potassium hydroxide in ethanol was further added and allowed to react for five minutes. The solid substance deposited after cooled on ice was filtered and washed with ethanol to obtain 8.24 g (23.1 mmol) of 7,9-diphenylcyclopenta[a]acenaphthylene-8-one. The yield was 71.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09028976B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-67ff0ccdf2d04779ba9e16d21b7f7d1e |
| Source note | uspto-grants-2015_05 |