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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165312Generated: November 1, 2026

Azobisisobutyronitrile → HCID 14423941, compound

https://huagongshe.com/reaction/2165312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 14423939HCID 14423939—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 14423941HCID 1442394193.4%

Reaction Steps

A slurry of 1,1-bis(4-fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-1-propene (61.46 g, 0.197 mole) [prepared in Step C], N-bromosuccinimide (35.06 g, 0.197 mole) and catalytic amount of azobis isobutyronitrile or benzoyl peroxide in carbon tetrachloride (1.2 liters) was heated to reflux in an inert atmosphere for a period of 2 hours. The reaction mixture was cooled to ambient temperature and the solid from the reaction was filtered. The filtrate was concentrated under reduced pressure and the solid obtained was recrystallized from toluene-hexane to give 72 g (93%) of the title compound as white crystals; m.p.=159°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939265
Source datasetuspto-grants-1990_07
ORD IDord-514248ef001b47b68f09448332675082
Source noteuspto-grants-1990_07