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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245319Generated: November 2, 2026

N-bromobutanimide → 5-[4-(Bromomethyl)phenyl]-2-ethyl-1,2,3,4-tetraazole

https://huagongshe.com/reaction/2245319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Ethyl-5-(4-methylphenyl)-1,2,3,4-tetraazoleHCID 20709932—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product5-[4-(Bromomethyl)phenyl]-2-ethyl-1,2,3,4-tetraazoleHCID 68682653103.7%

Reaction Steps

A solution of 18.8 grams (0.100 mole) of 2-ethyl-5-(4-methylphenyl)-1,2,3,4-tetraazole in 156 mL of carbon tetrachloride was stirred, and 19.6 grams (0.110 mole) of N-bromosuccinimide, followed by 0.24 gram (0.001 mole) of benzoyl peroxide were added. Upon completion of addition, the reaction mixture was heated to reflux where it stirred for 90 minutes. After this time the reaction mixture was cooled and filtered. The filtrate was concentrated under reduced pressure, yielding 27.7 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683070B2
Source datasetuspto-grants-2010_03
ORD IDord-feee1914c47f4592b66786ab9aa330c2
Source noteuspto-grants-2010_03