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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556841Generated: October 27, 2026

N-bromobutanimide → N-(5-bromo-4-chloropyridin-2-yl)-2,2-dimethylpropanamide

https://huagongshe.com/reaction/556841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN-(4-Chloropyridin-2-yl)pivalamideHCID 10656204—
SolventAcetonitrileHCID 6342—
ProductN-(5-bromo-4-chloropyridin-2-yl)-2,2-dimethylpropanamideHCID 5961342166.4%

Reaction Steps

NBS (8.37 g. 47.0 mmol) was added to a solution of N-(4-chloropyridin-2-yl)pivalamide (2.00 g, 9.40 mmol) in dry acetonitrile (20 mL). The resulting suspension was heated for 3 hr and then cooled to r.t. The solvent was removed in vacuo and the crude mixture was diluted with ethyl acetate (100 mL). The organic phase was washed with aqueous NaOH (10%, 2×40 mL), water (40 mL) and dried (MgSO4). The solvent was removed in vacuo and the crude mixture was purified by flash chromatography on silica, eluting with ethyl acetate and hexane (1/9), to give the title compound as a colourless solid (1.82 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058045B2
Source datasetuspto-grants-2011_11
ORD IDord-bc15ec3f196e42aeaa0742554446ad00
Source noteuspto-grants-2011_11