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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394313Generated: October 26, 2026

Water → 1-Boc-4-(2-pyridyloxy)piperidine

https://huagongshe.com/reaction/1394313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-BromopyridineHCID 7973—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDimethyl SulfoxideHCID 679—
SolventHexaneHCID 8058—
Product1-Boc-4-(2-pyridyloxy)piperidineHCID 2190603967%

Reaction Conditions

Temperature60 °C

Reaction Steps

60% sodium hydride (0.26 g, 6.5 mmol) was washed with hexane, and suspended in dry DMSO (10 mL). To the suspension was added a solution of 1-tert-butoxycarbonyl-4-hydroxypiperidine (1.01 g, 5.0 mmol) in dry DMSO (10 mL). The mixture was stirred at room temperature for 1 hour and at 60° C. for 1 hour, and cooled to room temperature. To the reaction mixture was added 2-bromopyridine (0.62 mL, 6.5 mmol), and the mixture was stirred at room temperature for 24 hours. To the reaction mixture was added water (50 mL), and the mixture was extracted with diethyl ether. The extract was washed with water and saturated aqueous solution of sodium hydrogen carbonate, successively, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (50 g, ethyl acetate-hexane 1:5) to give the titled compound as colorless crystals (928 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348324B2
Source datasetuspto-grants-2008_03
ORD IDord-e4c77281275a40e58e5d42c93fe473e5
Source noteuspto-grants-2008_03