Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055034Generated: October 30, 2026

Benzoyl Peroxide → AGN-PC-0NH77L

https://huagongshe.com/reaction/2055034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant[3-(2,4-diacetyloxyphenyl)-4-methyl-2-oxochromen-7-yl] acetateHCID 11200702—
CatalystTungstenHCID 23964—
SolventCarbon TetrachlorideHCID 5943—
ProductAGN-PC-0NH77LHCID 11179317—

Reaction Steps

A mixture of acetic acid 3-acetoxy-4-(7-acetoxy-4-methyl-2-oxo-2H-chromen-3-yl)phenyl ester (0.767 g, 1.87 mmol, 1 eq), N-bromosuccinimide (0.349 g, 1.962 mmol, 1.05 eq) and benzoyl peroxide (0.035 g, 0.145 mmol) in carbon tetrachloride (30 mL) was stirred and heated to reflux under nitrogen in presence of a 100 W tungsten lamp for 20 hours. Reaction monitoring by MS and TLC showed the presence unreacted starting material, and additional N-bromosuccinimide (0.060 g, 0.34 mmol) and benzoyl peroxide (0.008 g) were added to the reaction mixture and the reaction was heated at reflux under nitrogen for an additional 2 hours. The mixture was evaporated to dryness, dissolved in hot dichloromethane and purified by column chromatography on silica gel using 3% ethyl acetate/hexane as an eluent to yield the title product as a tan crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329654B2
Source datasetuspto-grants-2008_02
ORD IDord-1d7353cc62844920a890facb0a42a295
Source noteuspto-grants-2008_02