HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 68001716, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 68001708 | HCID 68001708 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68001716 | HCID 68001716 | 57.5% |
Reaction Steps
An amount of 6.8 g (20 mmol) of 3,4-dibromoacenaphthenequinone, 6.1 g (50 mmol) of phenylboronic acid, and 1 g of tetrakis triphenylphosphine palladium as catalysis were dissolved in a mixed solvent of 80 ml of toluene and 20 ml of ethanol. Then, 40 ml of 2M sodium carbonate solution was added and allowed to react at 90° C. for 12 hours. After the reaction was completed, the organic layer was separated and purified by column chromatography to obtain 3.85 g (11.5 mmol) of 3,4-diphenylacenaphthenequinone. The yield was 57.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09028976B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-4dee7911b1284499adbc7367e84c3543 |
| Source note | uspto-grants-2015_05 |