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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872556Generated: November 2, 2026

Benzoyl Peroxide → 5-Bromo-5-[3-(4-methoxyphenyl)propyl]barbituric acid

https://huagongshe.com/reaction/1872556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant5-[3-(4-Methoxyphenyl)propyl]barbituric acidHCID 14040670—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromo-5-[3-(4-methoxyphenyl)propyl]barbituric acidHCID 1840867987.1%

Reaction Steps

A mixture of 5-[3-(4-methoxyphenyl)propyl]barbituric acid (2.5 g), N-bromosuccinimide (2 g) and dibenzoyl peroxide (catalytic amount) in 110 ml of carbon tetrachloride is refluxed for about 1 hour then the solid which separated is filtered. The solid is redissolved in ethyl acetate and filtered through a silica gel cake in order to eliminate the succinimide residue. The organic phase is then concentrated to dryness and the residue is crystallized from diethylether/carbon tetrachloride mixture. A pale yellow solid separates which is filtered and dried under vacuum at 60° C. to give 2.8 g of the product. m.p. 113-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110924
Source datasetuspto-grants-2000_08
ORD IDord-783d7b0622f942c38944dc3baad962be
Source noteuspto-grants-2000_08