HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-(alpha-Bromoisopropyl) anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 13725949 | HCID 13725949 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(alpha-Bromoisopropyl) anthraquinone | HCID 53809179 | — |
Reaction Steps
A mixture of 0.95 g (3.8 mmol) 2-isopropylanthraquinone, 0.81 g (4.6 mmol) N-bromosuccinimide (NBS) and 6 mg benzoyl peroxide in 7 mL CCl4 was refluxed for 2 h under N2 with mild stirring. After cooling to room temperature, the solution was filtered through glass wool and then the CCl4 was removed under vacuum to yield a yellow liquid that solidified upon cooling. 1H-NMR showed the conversion to be complete and so the product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624543 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-04dcf34c559548e8be8ef5d2f1cd8a51 |
| Source note | uspto-grants-1997_04 |