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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591653Generated: November 1, 2026

Water → Tert-butyl 1-[3-(4-cyanophenoxy)propyl]-4-piperidinylcarbamate

https://huagongshe.com/reaction/1591653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantHCID 10879224HCID 10879224—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 1-[3-(4-cyanophenoxy)propyl]-4-piperidinylcarbamateHCID 2303395782%

Reaction Steps

1.44 g of 4-tert-butoxycarbonylaminopiperidine was dissolved in 14 ml of N,N-dimethylformamide. Thereafter, 1.99 g of potassium carbonate and 1.87 g of 4-(3-bromopropoxy)benzonitrile were successively added to the above solution, followed by stirring at room temperature for 24 hours. Water and ethyl acetate were added to the reaction mixture, so that the organic layer was separated. The separated organic layer was washed with a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. Thereafter, the solvent was removed under a reduced pressure. The obtained solid was filtrated with a mixed solution consising of n-hexane and diisopropyl ether to obtain 2.12 g of tert-butyl 1-[3-(4-cyanophenoxy)propyl]-4-piperidinylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291617B2
Source datasetuspto-grants-2007_11
ORD IDord-34d304883b254b109aeb0a7cca8057da
Source noteuspto-grants-2007_11