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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962836Generated: October 30, 2026

Hydrochloric Acid → 2,6-Dibromo-3,5-dimethoxypyridine

https://huagongshe.com/reaction/1962836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantSodium SulfiteHCID 24437—
ReactantPotassium BromideHCID 253877—
Reactant3,5-DimethoxypyridineHCID 817733—
ReactantPotassium BromateHCID 23673461—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product2,6-Dibromo-3,5-dimethoxypyridineHCID 335798983.9%

Reaction Steps

A flask was charged with 3,5-dimethoxypyridine (13 g; 93 mmol), water (100 mL) and concentrated hydrochloric acid (8 mL; ˜1 eq.). To a separate flask was added potassium bromide (65 g.), water (200 mL) and sulfuric acid (69 g.). To a third flask was added potassium bromate (18 g.), and water (1.2 liters). All flasks were stirred until they were homogenous. To the flask with potassium bromate was added the solution containing potassium bromide, followed by the solution containing the pyridine compound. The reaction was stirred for ten minutes, and a solution of sodium sulfite was added until the orange color disappeared. The solid was collected by Buchner funnel, washed with water, dissolved in dichloromethane, dried over sodium sulfate, and evaporated to give 2,6-dibromo-3,5-dimethoxypyridine (23.3 g; 78 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415377B2
Source datasetuspto-grants-2013_04
ORD IDord-2c4bae337f7144bdae247ddd464db68f
Source noteuspto-grants-2013_04