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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066894Generated: October 25, 2026

Ethanol → 4-(Piperidin-4-ylideneaminooxy)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2066894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-PiperidoneHCID 33721—
ReactantSodium AcetateHCID 517045—
Reactanttert-Butyl 4-(aminooxy)piperidine-1-carboxylateHCID 24729482—
SolventDichloromethaneHCID 6344—
Product4-(Piperidin-4-ylideneaminooxy)-piperidine-1-carboxylic acid tert-butyl esterHCID 5833359899.2%

Reaction Steps

To a solution of 4-piperidinone (2.5 mmol) in 25 mL of DCM, was added 69b (0.43 g, 2 mmol). The mixture was stirred at room temperature for 2 h. NaOAc (0.27 g, 2 mmol) and ethanol (10 mL) were added and the reaction mixture was heated at 70° C. for 2 h. The solution was allowed to cool down to room temperature and the ethanol was evaporated. The residue was extracted with ethyl acetate, washed with water, dried and concentrated to give 0.59 g of 69c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293729B2
Source datasetuspto-grants-2012_10
ORD IDord-18f80c420105424ab0f2180faf278b0b
Source noteuspto-grants-2012_10