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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763938Generated: November 2, 2026

Benzoyl Peroxide → HCID 12401525, compound

https://huagongshe.com/reaction/1763938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant[1,2,4]Triazolo[1,5-a]pyridine, 2-(4-methylphenyl)-HCID 12308360—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 12401525HCID 12401525—

Reaction Conditions

Temperature20 °C

Reaction Steps

41.85 g of 2-(p-tolyl)-s-triazolo[1,5-a]pyridine (26) are dissolved at 50° C. in 1,200 ml of dry carbon tetrachloride. 37.4 g of N-bromosuccinimide and 1 g of dibenzoyl peroxide are then added and the mixture is warmed gradually to the boil while stirring well and with exposure to a 400 W lamp. The reaction mixture is kept under reflux for 4 hours and is then cooled to 20° C. and the product which has precipitated is filtered off with suction. The succinimide is removed by washing with a large amount of water and the material on the suction filter is dried. This gives 39.2 g (58% of theory) of compound (I) in the form of a pale beige powder with a melting point of 192° to 193° C. After recrystallising twice from toluene, 32.3 g (56.1% of theory) of small, virtually colourless, glossy needles with a melting point of 195.5° to 196° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113937
Source datasetuspto-grants-1978_09
ORD IDord-9d836d5c00654700be96133baaf83927
Source noteuspto-grants-1978_09