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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273911Generated: November 3, 2026

Ethylene Glycol → tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2273911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant4-IodoanilineHCID 10893—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
CatalystCopper iodideHCID 83717—
SolventIsopropanolHCID 3776—
Producttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 1101130143.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-iodoaniline (0.654 g, 3 mmol), piperazine-1-carboxylic acid tert-butyl ester (0.67 g, 3.6 mmol), potassium phosphate (1.272 g, 6 mmol), ethylene glycol (0.33 ml) and copper iodide (0.03 g, 0.15 mmol) in 2-propanol (3 ml) was placed under argon in a sealed-tube and heated to 80° C. for 30 hours. After being cooled to room temperature, the medium was washed with water (50 ml) and extracted with ethyl acetate (100 ml). The organic layer was dried over MgSO4, concentrated and chromatographed (dichloromethane:acetone, 70:30) to yield 43a (0.36 g, 1.3 mmol, 43%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126941B2
Source datasetuspto-grants-2015_09
ORD IDord-abd03e79c8244309a08a743b9123352f
Source noteuspto-grants-2015_09