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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779135Generated: November 2, 2026

2,6-Dibromopyridine → 2,6-Bis(2,2,6,6-tetramethylpiperidin-1-yl)pyridine

https://huagongshe.com/reaction/1779135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DibromopyridineHCID 12274—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantPotassium bis-trimethylsilylamideHCID 86585346—
Solvent1,4-DioxaneHCID 31275—
Product2,6-Bis(2,2,6,6-tetramethylpiperidin-1-yl)pyridineHCID 67609574—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 1,4-dioxane solution (30 ml) of 2,2,6,6-tetramethylpiperidine (3.11 g, 22.0 mmol) and potassium-bis(trimethylsilyl)amide (4.39 g, 22.0 mmol)2 was added 2,6-dibromopyridine (2.37 g, 10.0 mmol). The reaction mixture was stirred vigorously at 100° C. overnight. After cooling down to room temperature, the reaction was quenched with water and extracted with diethyl ether/THF (1:1) mixtures. The combined extracts were washed with 1 M Na2CO3, dried over MgSO4, filtrated, and evaporated to dryness. The product was purified by flash chromatography on silica gel leading to colorless oil (Rf=0.5 in Ethylacetate:hexane=1:20, Yield=1.13 g (31.6%))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09269912B2
Source datasetuspto-grants-2016_02
ORD IDord-c3335102052743728ff378f989d3f90a
Source noteuspto-grants-2016_02