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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54867Generated: October 28, 2026

Benzoyl Peroxide → 2-(alpha-Bromoisopropyl) anthraquinone

https://huagongshe.com/reaction/54867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 13725949HCID 13725949—
SolventCarbon TetrachlorideHCID 5943—
Product2-(alpha-Bromoisopropyl) anthraquinoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624543
Source datasetuspto-grants-1997_04
ORD IDord-04dcf34c559548e8be8ef5d2f1cd8a51
Source noteuspto-grants-1997_04