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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380153Generated: October 31, 2026

Benzoyl Peroxide → HCID 54452167, compound

https://huagongshe.com/reaction/2380153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantBromineHCID 24408—
Reactant(4-Methoxyphenyl)(3-methylphenyl)methanoneHCID 12469466—
Solvent1,2-DibromoethaneHCID 7839—
ProductHCID 54452167HCID 5445216760.8%

Reaction Steps

A solution of the benzophenone (17.5 g, 77.4 mmole) of Step A in ethylene bromide (26.5 mL) (containing a small amount of benzoyl peroxide) is heated at reflux. A solution of bromine (12.7 g, 79.6 mmole) in ethylene bromide (15 mL) is added dropwise over 30 minutes while the mixture is irradiated with a Photolamp (300 W). Reflux is continued for 17 hours (TLC, 9:1 petrolether-ethylacetate, traces of starting material still present). The solvent is removed in vacuo and the residue (brown oil, 39.22 g) is purified by flask chromatography (on silica Merck-60, preabsorbed in dichloromethane, eluted with 9:1 petrolether-ethyl acetate) to give unreacted starting material (2.59 g, ca.. 15%) along with the desired product (14.36 g, 61% or 71.5% based on recovered unreacted starting material) and some mixed fractions (ca. 5.20 g). The light yellow solid melts at 58°-61 ° C. and it is used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364944
Source datasetuspto-grants-1994_11
ORD IDord-fff8af551f3a4b94a16e774522e12941
Source noteuspto-grants-1994_11