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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357930Generated: October 30, 2026

N-bromobutanimide → 2,3-Dibromo-6-methoxypyridine

https://huagongshe.com/reaction/2357930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-6-methoxypyridineHCID 256810—
SolventAcetonitrileHCID 6342—
Product2,3-Dibromo-6-methoxypyridineHCID 59389317—

Reaction Conditions

Temperature85 °C

Reaction Steps

NBS (302 g) was added to the compound of Example 259 (295 g) in acetonitrile (575 mL) and the mixture was stirred at 80 to 90° C. for 1 day in a nitrogen atmosphere. After cooling, the crystallized imide was removed by filtration and the filtrate was concentrated. Purification of the resulting residue by silica gel column chromatography (ether:petroleum ether=1:1) gave a 6:1 mixture of the title compound and 2,5-dibromo form. This product was crystallized from cold petroleum ether to afford the title compound as a colorless powder (223 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763617B2
Source datasetuspto-grants-2010_07
ORD IDord-93ee9fdcf12b4cd785e0e92176f5cd17
Source noteuspto-grants-2010_07