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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656293Generated: October 28, 2026

N-bromobutanimide → N-[6-(Bromomethyl)pyridin-2-yl]-2,2-dimethylpropanamide

https://huagongshe.com/reaction/656293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN-(6-Methylpyridin-2-yl)pivalamideHCID 3251458—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductN-[6-(Bromomethyl)pyridin-2-yl]-2,2-dimethylpropanamideHCID 143267065%

Reaction Steps

2,2 ethyl-N-(6-methyl-2-pyridinyl)propaneamide (21-1) (32 g) and N-bromosuccinimide (29.6 g) were added to carbon tetrachloride (300 ml) and to the mixture was added AIBN (15 mg), followed by reluxing for 20 hours under light emitted by 500 W lamp. The resulting mixture was cooled to room temperature, filtered, and concentrated under reduced pressure. The residue was purified by column-chromatography (hexane/ethyl acetate=10/1) to yield the compound 21-2 (1.94 g, 5%) as a pure white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071650B2
Source datasetuspto-grants-2011_12
ORD IDord-992db61ff61e4a0290ab8a231e1f7778
Source noteuspto-grants-2011_12