Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601027Generated: October 25, 2026

1,2-Dichloroethane → Tert-butyl 4-(4-aminobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/601027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-Aminobenzoic AcidHCID 978—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(4-aminobenzoyl)piperazine-1-carboxylateHCID 276335587%

Reaction Steps

To a solution of 4-aminobenzoic acid (411 mg, 3.00 mmol) in DMF (3.0 mL) at room temperature was added EDC (862 mg, 4.50 mmol), HOBt (608 mg, 4.50 mm01), triethylamine (606 mg, 0.835 mL, 6.00 mmol) and tert-butyl piperazinecarboxylate (671 mg, 3.60 mmol). The mixture was stirred for 22 h, and then 2 N aq. NaOH was added to adjust the PH>10. The mixture was extracted with ethyl acetate, and the organic layer was dried over MgSO4, concentrated. The residue was purified by silica gel column chromatograghy eluted with EtOAc:hexanes (50 to 90% EtOAc) to give 4-(4-amino-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester (796 mg, 87%) as a colorless oil. MS (ES+): m/z=306.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902239B2
Source datasetuspto-grants-2011_03
ORD IDord-ec90e0f76d94466181e9cebac0f2632c
Source noteuspto-grants-2011_03