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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244442Generated: October 31, 2026

Sodium hydride → 5-Chloro-2-(piperidin-4-yloxy)pyridine

https://huagongshe.com/reaction/1244442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,5-DichloropyridineHCID 27685—
ReactantPiperidin-4-olHCID 79341—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-Chloro-2-(piperidin-4-yloxy)pyridineHCID 11264329—

Reaction Conditions

Temperature82 °C

Reaction Steps

NaH (2.88 g, 66 mmol, 55% dispersion in mineral oil) was stirred in dry DME (200 ml), under Argon. A mixture of 2,5-dichloropyridine (8.87 g, 60 mmol) and 4-hydroxypiperidine (6.67 g, 66 mmol) dissolved in dry DME (200 ml) was added to the NaH suspension dropwise, over a period of 30 minutes. After complete addition the reaction is heated to 82° C. for 48 hrs, maintaining the Argon blanket. The reaction was slowly quenched with water before removing most of the THF. Extracted the aqueous with DCM (×3). The organic layers were dried with Na2SO4 and evaporated in vacuo to afford 2-(4-piperidinyloxy)-5-chloropyridine as a yellow oil (12.7 g, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122551B2
Source datasetuspto-grants-2006_10
ORD IDord-e6e201fbab1a4da5bd56586f149849e3
Source noteuspto-grants-2006_10