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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621738Generated: October 31, 2026

Azobisisobutyronitrile → HCID 14423941, compound

https://huagongshe.com/reaction/621738

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 numberUS04824959
Source datasetuspto-grants-1989_04
ORD IDord-d827c9eec65f41a1ba69ddf14b6259a1
Source noteuspto-grants-1989_04