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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255533Generated: November 1, 2026

Azobisisobutyronitrile → HCID 131718089, compound

https://huagongshe.com/reaction/2255533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 131718090HCID 131718090—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 131718089HCID 131718089—

Reaction Steps

To a solution of N-Triphenylmethyl-5-(4-fluoro-4'-methyl-biphen-2-yl)tetrazole (454.4 mg; 0.9161 mmol) in dry CCl4 (8 mL) was added N-bromosuccinimide (179.2 mg; 1.1 eq) and a catalytic amount of AIBN. The reaction was heated to reflux (105°-115°) under N2. After 3 hrs. the reaction was cooled and filtered through a cotton plugged pipet to remove the succinimide formed. The solvent was removed and replaced by EtOAc/Et2O. The reaction was washed with 1N NaOH and brine. The organic solution was dried over anhydrous MgSO4, filtered, and concentrated in vacuo to afford the product. The crude product was used in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240928
Source datasetuspto-grants-1993_08
ORD IDord-4138e63ce9414e8cb4788aea39893571
Source noteuspto-grants-1993_08