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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726623Generated: October 30, 2026

Hydrochloric Acid → 5-Bromo-2-chloro-4,6-dimethylnicotinonitrile

https://huagongshe.com/reaction/726623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178433466HCID 178433466—
CatalystDimethylformamideHCID 6228—
SolventPhosphorus oxychlorideHCID 24813—
Product5-Bromo-2-chloro-4,6-dimethylnicotinonitrileHCID 2763844—

Reaction Steps

A mixture of 9.0 grams (0.040 mole) of 5-bromo-3-cyano-2-hydroxy-4,6-dimethylpyridine in 40 mL of phosphorus oxychloride is stirred, and one drop (catalyst) of N,N-dimethylformamide is added. The reaction mixture is then stirred at ambient temperature for about five hours, and then allowed to stand for about 72 hours. After this time, the reaction mixture is poured into 1000 mL of ice containing about one mL of concentrated hydrochloric acid. The mixture is stirred until the ice melts. The resultant precipitate is collected by filtration and washed with water. The solid is then dried under reduced pressure at about 60° C. An NMR spectrum of the solid indicates that it contains a large amount of starting material. The solid is then dissolved in 25 mL of phosphorus oxychloride, and two drops of N,N-dimethylformamide are added. The mixture is heated to reflux where it is stirred for about 18 hours. After this time, the reaction mixture is poured into 600 mL of ice containing about two mL of concentrated hydrochloric acid. The mixture is stirred until the ice melts. The resultant precipitate is collected by filtration, washed with water, and dried under reduced pressure at about 60° C., yielding 8.6 grams of 5-bromo-2-chloro-3-cyano-4,6-dimethylpyridine. The NMR spectrum is consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710157
Source datasetuspto-grants-1998_01
ORD IDord-30bc8f063a4c4b96854a60a973807889
Source noteuspto-grants-1998_01