Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627556Generated: October 30, 2026

Sodium hydride → HCID 11149549, compound

https://huagongshe.com/reaction/1627556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,5-DibromopyridineHCID 69353—
ReactantPiperidin-4-olHCID 79341—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 11149549HCID 1114954958%

Reaction Steps

Sodium hydride (56 mg, 2.3 mmol) was added to a solution of piperidin-4-ol (214 mg, 2.11 mmol) in DMSO (8 mL). After stirring for 30 minutes, 2,5-dibromopyridine was added. After stirring for 24 hours, sodium hydride (56 mg, 2.3 mmol) was added. After stirring for another 24 hours the reaction was partitioned between ethyl acetate and water. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over MgSO4 and concentrated by rotary evaporation. The residue was purified by silica gel chromatography using gradient elution of dichloromethane, methanol, ammonium hydroxide to afford 5-bromo-2-(piperidin-4-yloxy)-pyridine (316 mg, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785632B2
Source datasetuspto-grants-2014_07
ORD IDord-f5b7b399bd8941f299303e317472bca3
Source noteuspto-grants-2014_07