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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467987Generated: October 26, 2026

2,6-Dichloropyridine → Tert-butyl 4-[(6-chloropyridin-2-yl)oxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/1467987

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichloropyridineHCID 16989—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-[(6-chloropyridin-2-yl)oxy]piperidine-1-carboxylateHCID 2190605848%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 4-Hydroxy-piperidine-1-carboxylic acid tert-butyl ester (1.63 g, 8.1 mmol) in THF (20 mL), NaH (0.40 g, 10.1 mmol)) was added and stirred at 60° C. for 0.5 h. 2,6-dichloropyridine (1.0 g, 6.75 mmol) was added and stirred at room temperature for 3-4-h. The reaction was quenched with water and extracted with ethyl acetate. The organic layer was concentrated in vacuo and the resultant residue was purified by flash column chromatography to yield tert-butyl 4-((6-chloropyridin-2-yl)oxy)piperidine-1-carboxylate as a pale yellow solid (0.98 g, 48%); MS: 335.1 (M+23)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000175B2
Source datasetuspto-grants-2015_04
ORD IDord-6b98d450d34d4947afe804c798f92a1c
Source noteuspto-grants-2015_04