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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856033Generated: October 30, 2026

Tert-butyl(4-benzylpiperazin-1-yl)carbamate → tert-Butyl piperazin-1-ylcarbamate

https://huagongshe.com/reaction/856033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl(4-benzylpiperazin-1-yl)carbamateHCID 23081385—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Producttert-Butyl piperazin-1-ylcarbamateHCID 2170165899%

Reaction Steps

Tert-butyl(4-benzylpiperazin-1-yl)carbamate (42.22 g, 145 mmol) prepared in Reference Example 35 was dissolved in ethanol (300 ml). To which 20% palladium hydroxide/carbon (6.0 g) was added, and the mixture was stirred at room temperature under an atmospheric pressure of hydrogen for 20 minutes, and then at 50° C. for 30 minutes. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. Thus obtained solid was washed with IPE, collected by filtration, and dried under reduced pressure to afford tert-butyl piperazin-1-yl-carbamate (28.9 g, yield 99%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-88382c786981466c9830c93761e911bd
Source noteuspto-grants-2007_08