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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335149Generated: October 29, 2026

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

https://huagongshe.com/reaction/335149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-[hydroxy(pyridin-2-yl)methyl]piperidine-1-carboxylateHCID 1853909233.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Placed 2-bromopyridine (0.833 g, 5.27 mmol) in THF (25 mL) and cooled to −78° C. Butyllithium (2.11 mL, 5.27 mmol) was slowly added and stirred for 5 minutes. Dissolved tert-butyl 4-formylpiperidine-1-carboxylate (0.500 g, 2.34 mmol) in THF (3 mL) and added slowly to the above solution then stirred at −78° C. for 30 minutes. Added ammonium chloride and extracted with CH2Cl2. Concentrated and purified by silica gel to give the title compound (0.229 g, 33.4% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883828B2
Source datasetuspto-grants-2014_11
ORD IDord-edd926cdec824facb61cb63a39f242c2
Source noteuspto-grants-2014_11