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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885836Generated: October 31, 2026

p-Toluenesulfonic acid → 2-Bromo-5-(dimethoxymethyl)pyridine

https://huagongshe.com/reaction/885836

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
SolventMethanolHCID 887—
Product2-Bromo-5-(dimethoxymethyl)pyridineHCID 642521395.6%

Reaction Steps

A solution of 6-bromopyridine-3-carbaldehyde (3.07 g, 16.5 mmol), p-toluenesulfonic acid (386 mg, 2.02 mmol) and trimethyl orthoformate (1.97 ml, 18 mmol) in MeOH (80 ml) was stirred at room temperature for 48 hours. The mixture was then brought to basic conditions with a 5% NaHCO3 solution and extracted twice with diethyl ether. The pooled organic phases were dried over Na2SO4 and evaporated to dryness to give 3.66 g of 2-bromo-5-dimethoxymethyl-pyridine as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242175B2
Source datasetuspto-grants-2012_08
ORD IDord-da5f42b359da4c28b399296303b378bb
Source noteuspto-grants-2012_08