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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792456Generated: November 4, 2026

2,5-Dibromopyridine → 5-Bromo-N-(2,2-dimethoxyethyl)pyridin-2-amine

https://huagongshe.com/reaction/1792456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DibromopyridineHCID 69353—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantSodium BicarbonateHCID 516892—
Product5-Bromo-N-(2,2-dimethoxyethyl)pyridin-2-amineHCID 16414251—

Reaction Steps

After 50 g of 2,5-dibromopyridine and 50 mL aminoacetaldehyde dimethyl acetal were heated at 130° C. for 8 hours, an aqueous saturated sodium bicarbonate solution was added thereto, and the reaction mixture was extracted with ethyl acetate. The extract was washed with brine, the organic layer was dried over anhydrous sodium sulfate, the solvent was removed, and the resulting crude product was purified by silica gel column chromatography (ethyl acetate/hexane), to give 23.53 g of the title compound (pale yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074801B1
Source datasetuspto-grants-2006_07
ORD IDord-7826fd182752414c9f1a1263d827f13b
Source noteuspto-grants-2006_07