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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974482Generated: October 29, 2026

Azobisisobutyronitrile → HCID 14423941, compound

https://huagongshe.com/reaction/974482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-BromosuccinamideHCID 9834204—
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-bromosuccinamide (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 numberUS05068346
Source datasetuspto-grants-1991_11
ORD IDord-b3cf8cf621944dc7906d534c4d56f5ac
Source noteuspto-grants-1991_11