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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267968Generated: October 30, 2026

Benzoyl Peroxide → HCID 18348173, compound

https://huagongshe.com/reaction/2267968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 18348181HCID 18348181—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18348173HCID 1834817315.9%

Reaction Steps

Under a light source a stirred solution of 2.8 grams (0.013 mole) of 1-(2-fluoroethyl)-4-(4-methylphenyl)-1,2,3,5-(1H)-tetrazole, 2.4 grams (0.013 mole) of N-bromosuccinimide, and 0.19 gram (0.0008 mole) of benzoyl peroxide in 100 mL of carbon tetrachloride was heated to reflux. Once at reflux the reaction mixture was stirred for five hours. After this time the heat source was removed and the reaction mixture was stirred for about 18 hours. At the conclusion of this period the reaction mixture was filtered, and the filtrate was concentrated under reduced pressure, yielding 0.59 gram of 4-[1-(2-fluoroethyl)-1,2,3,5-(1H)-tetrazol-4-yl]benzyl bromide. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0002007H1
Source datasetuspto-grants-2001_12
ORD IDord-7cc0d601b10641d9927ccf8cb976ded7
Source noteuspto-grants-2001_12