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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290802Generated: November 1, 2026

Benzoyl Peroxide → 7-(1-Bromoethyl)-1,2,4-triazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1290802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Ethyl-1,2,4-triazolo[1,5-a]pyrimidineHCID 18919353—
SolventCarbon TetrachlorideHCID 5943—
Product7-(1-Bromoethyl)-1,2,4-triazolo[1,5-a]pyrimidineHCID 18919351—

Reaction Steps

A mixture of 7-ethyl-1,2,4-triazolo[1,5-a]pyrimidine (10.5 g), N-bromosuccinimide (12.63 g), dibenzoylperoxide (0.3 g) and tetrachloromethane (270 ml) was heated under reflux for 5 hours with stirring. The mixture was filtered and a crude product was obtained by evaporation of the solvent from the filtrate. This was purified by recrystallisation from tetrachloromethane to give 7-(1-bromoethyl)-1,2,4-triazolo[1,5-a]pyrimidine. Yield 10.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753665
Source datasetuspto-grants-1998_05
ORD IDord-500a3da8126445c6a19de442eeceb3b4
Source noteuspto-grants-1998_05