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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398086Generated: November 2, 2026

2-Chloro-5-nitropyridine → 1-(5-nitropyridin-2-yl)piperidin-4-ol

https://huagongshe.com/reaction/1398086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantPiperidin-4-olHCID 79341—
Solvent1-PropanolHCID 1031—
Product1-(5-nitropyridin-2-yl)piperidin-4-olHCID 285976897.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 1.0 g (6.3 mmol) of 2-chloro-5-nitropyridine in 20 mL of n-propanol was added 1.9 g (18.9 mmol) of 4-hydroxypiperidine, and the mixture was stirred for 1.5 hours at 100° C. After cooling the reaction mixture, the solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: dichloromethane/methanol=50/1) to give 1.37 g (97%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901315B2
Source datasetuspto-grants-2014_12
ORD IDord-8c584e5e3dbc45c39b6f63ef870d1708
Source noteuspto-grants-2014_12