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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097244Generated: October 31, 2026

Acetic Acid → 2-Bromo-6-piperidin-1-ylmethylpyridine

https://huagongshe.com/reaction/1097244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product2-Bromo-6-piperidin-1-ylmethylpyridineHCID 1378454487.1%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 6-bromopyridine-2-carbaldehyde (25 g, 135 mmol) in dichloromethane (500 ml) was slowly added piperidine (12.6 g, 149 mmol) at 10° C. After stirring for 15 minutes at 10° C., acetic acid (8.9 g, 149 mmol) was added, followed by the portionwise addition of sodium triacetoxyborohydride, while the temperature was kept at 5-10° C. After stirring for 2 h at room temperature the reaction mixture was poured into a saturated aqueous solution of sodium hydrogen carbonate. The product was extracted into dichloromethane and the combined organic phases were washed with brine, dried over sodium sulphate and concentrated under reduced pressure. Column chromatography afforded 2-bromo-6-(piperidin-1-ylmethyl)pyridine (30 g) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143246B2
Source datasetuspto-grants-2012_03
ORD IDord-5a6bcd1685844117ae293904b94b0d1f
Source noteuspto-grants-2012_03