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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374739Generated: October 29, 2026

1,1-Dimethylethyl 2-(2-hydroxyethyl)-4-(phenylmethyl)-1-piperazinecarboxylate → tert-Butyl 2-(2-hydroxyethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1374739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl 2-(2-hydroxyethyl)-4-(phenylmethyl)-1-piperazinecarboxylateHCID 18932955—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 2-(2-hydroxyethyl)piperazine-1-carboxylateHCID 1893303892%

Reaction Steps

A solution of (RS)-4-benzyl-1-(tert-butyloxycarbonyl)-2-(2-hydroxyethyl)piperazine (D5) (2.5 g, 7.81 mmol) in ethanol (150 ml) was hydrogenated at atmospheric pressure and room temperature in the presence of 10% palladium on charcoal (2.07 g, 54% paste with water) for 3.5 h. The mixture was filtered through Kieselguhr and the filtrate evaporated in vacuo to give the title compound as a colourless oil (1.65 g, 92%). Mass spectrum (AP+): Found 231 (MH+). C11H22N2O3 requires 230.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166608B2
Source datasetuspto-grants-2007_01
ORD IDord-03afa0d63fe742f9a54925be90c73f95
Source noteuspto-grants-2007_01