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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412894Generated: October 29, 2026

2-Bromopyridine → tert-Butyl 4-[hydroxy(pyridin-2-yl)methyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/412894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 4-[hydroxy(pyridin-2-yl)methyl]piperidine-1-carboxylateHCID 1853909262%

Reaction Steps

To a solution of 2-bromopyridine (488 μL, 5 mmol) in ether (10 mL) was added dropwise butyl lithium (1.6M hexane solution, 3.125 mL, 5 mmol) at −78° C., and the mixture was stirred for 30 minutes. To the mixture was added dropwise a solution of 1-tert-butoxycarbonyl-4-formylpiperidine (1066 mg, 5 mmol) in ether (10 mL) at −78° C. The mixture was stirred for 18 hours while the temperature is elevated to room temperature. The reaction mixture was washed with saturated aqueous solution of sodium hydrogencarbonate and saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography (ethyl acetate:hexane=1:2) to give the titled compound as yellowish oily substance (913 mg). Yield 62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562978B1
Source datasetuspto-grants-2003_05
ORD IDord-bc68ff9b117b4c3a9dae0cb6b95aabb2
Source noteuspto-grants-2003_05