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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993664Generated: October 31, 2026

Cesium carbonate → 1,1-Dimethylethyl 4-[(4-nitro-2-pyridinyl)oxy]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1993664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant2-Chloro-4-nitropyridineHCID 735152—
Reactant(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product1,1-Dimethylethyl 4-[(4-nitro-2-pyridinyl)oxy]-1-piperidinecarboxylateHCID 68538021—

Reaction Steps

Add 100 mL of toluene to a nitrogen purged mixture of 2-chloro-4-nitro-pyridine (4.32 g, 27.2 mmol), tert-butyl 4-hydroxypiperidine carboxylate (11.0 g, 54.5 mmol), cesium carbonate (13.3 g, 40.8 mmol), palladium acetate (122 mg, 0.544 mmol) and 2-(di-tert-butylphosphino)-1,1′-binapthyl (271 mg, 0.68 mmol). Stir the resulting mixture overnight at room temperature, then partition between water and ethyl acetate. Extract the aqueous layer with additional ethyl acetate, and dry the combined organic layer over sodium sulfate and concentrate under reduced pressure. Subject residue to silica gel chromatography eluting with a gradient of 0 to 20% ethyl acetate in hexanes to afford 4-(4-nitro-pyridin-2-yloxy)-piperidine-1-carboxylic acid tert-butyl ester as a white waxy solid (5.37 g, 61%; LCMS ES+(m/z) 268 [M-tBu]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652015B2
Source datasetuspto-grants-2010_01
ORD IDord-aee9de94020a42c59a4939777f686770
Source noteuspto-grants-2010_01