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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861995Generated: October 29, 2026

Azobisisobutyronitrile → HCID 12187011, compound

https://huagongshe.com/reaction/861995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantN-(6-Methylpyridin-2-yl)pivalamideHCID 3251458—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 12187011HCID 1218701147%
ProductN-[6-(Bromomethyl)pyridin-2-yl]-2,2-dimethylpropanamideHCID 1432670633%

Reaction Steps

Carbontetrachloride (CCl4, 300 mL) and the product of Example 1 (50.6 g, 0.26 mol) were added to a 1 L flask equipped with a N2 inlet The solution was stirred until all solid dissolved. N-bromo-succinimide (NBS, 46.8 g, 0.26 mol) was then added to the reaction flask, followed by 2,2'-azobisisobutyronitrile (AIBN, 0.02 g). The reaction was heated to reflux for 6 h with a 500 watt reflector spot lamp. An additional 0.5 eq (23.4 g) of NBS was added to the reaction, and refluxing was continued for 2 h. After cooling the reaction to room temperature, it was filtered and all solvent was removed under reduced pressure. Flash chromatography (15/85 EtOAc/Hex) provided 31.6 g (47%) of title product and 22.2 g (33%) of the title material of Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716964
Source datasetuspto-grants-1998_02
ORD IDord-a13d8f64444b4a6fa60c199ffb654212
Source noteuspto-grants-1998_02