HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dibromopyridine → 2,6-Bis(2,2,6,6-tetramethylpiperidin-1-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | Potassium bis-trimethylsilylamide | HCID 86585346 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,6-Bis(2,2,6,6-tetramethylpiperidin-1-yl)pyridine | HCID 67609574 | — |
Reaction Conditions
| Temperature | 100 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09269912B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-c3335102052743728ff378f989d3f90a |
| Source note | uspto-grants-2016_02 |