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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706498Generated: October 30, 2026

Benzoyl Peroxide → 1-Phenyl-3-(o-anisyloxy)propylbromide

https://huagongshe.com/reaction/1706498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Methoxy-2-[(3-phenylpropoxy)methyl]benzeneHCID 15208420—
SolventCarbon TetrachlorideHCID 5943—
Product1-Phenyl-3-(o-anisyloxy)propylbromideHCID 20336045—

Reaction Steps

Using a similar procedure to that above, a reaction mixture was prepared containing 48 g. of N-bromosuccinimide, 65 g. of 1-phenyl-3-(o-anisyloxy)propane and 300 ml. of carbon tetrachloride. 500 mg. of benzoyl peroxide were added and the resulting mixture heated at reflux for about 2 hours at which point thin-layer chromatography indicated that no starting material remained in the reaction mixture. The reaction mixture was cooled, the succinimide separated by filtration and the solvent removed from the filtrate by evaporation in vacuo. A residual oil weighing about 88 g. comprising 1-phenyl-3-(o-anisyloxy)propylbromide formed in the above reaction was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207343
Source datasetuspto-grants-1980_06
ORD IDord-4ac83b515d464eeabfe186be56067547
Source noteuspto-grants-1980_06