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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922706Generated: October 29, 2026

HCID 59605421, compound → 1-tert-Butyl-2-piperazinone

https://huagongshe.com/reaction/1922706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59605421HCID 59605421—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-tert-Butyl-2-piperazinoneHCID 2308108469%

Reaction Steps

A 10 mL round-bottomed flask was charged with a solution of 4-tert-butyl-3-oxopiperazine-1-carboxylic acid benzyl ester (0.75 g, 2.58 mmol) in EtOH (5 mL). The reaction mixture was flushed with nitrogen and 10% Pd/C (67 mg, 0.13 mmol) was added. The reaction mixture was stirred under a hydrogen atmosphere for 18 h. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge. The cartridge was washed with MeOH and the desired product was eluted using 2 M NH3 in MeOH to give 1-tert-Butylpiperazin-2-one as grey oil (0.276 g, 69%). 1H NMR (300 MHz, CDCl3): δ 3.50 (s, 2H), 3.37 (t, J=5.5 Hz, 2H), 3.06 (t, J=5.5 Hz, 2H), 1.48-1.41 (m, 9H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173650B2
Source datasetuspto-grants-2012_05
ORD IDord-86fb305c1b3c44b8936c4d07b4e2312c
Source noteuspto-grants-2012_05