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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638563Generated: October 31, 2026

Azobisisobutyronitrile → HCID 19841102, compound

https://huagongshe.com/reaction/1638563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 19841104HCID 19841104—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 19841102HCID 1984110269%

Reaction Steps

To a mixture 0.55 g of 2-butyl-1-[(2'-carboxymethylbiphenyl-4-yl)methyl]benzimidazole-6-carboxaldehyde in 30 mL of carbon tetrachloride was added 0.23 g of N-bromosuccinimide and a catalytic amount of azobisisobutyronitrile. The reaction was stirred at room temperature until the reaction went to completion and then concentrated to dryness. The residue was partitioned between ethyl acetate and water. The organic phase was washed with water, dried and concentrated. Flash column chromatography (silica gel; 1:1 hexane/ethyl acetate to 1:3 hexane/ethyl acetate) afforded 0.45 g of the product as a thick clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880804
Source datasetuspto-grants-1989_11
ORD IDord-2ba6901a340947cf80c180fe9aa56db6
Source noteuspto-grants-1989_11