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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473816Generated: October 31, 2026

Benzyl chloroformate → 1-Benzyl 4-tert-butyl 2-phenylpiperazine-1,4-dicarboxylate

https://huagongshe.com/reaction/473816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl 3-phenylpiperazine-1-carboxylateHCID 2735358—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product1-Benzyl 4-tert-butyl 2-phenylpiperazine-1,4-dicarboxylateHCID 6751457059%

Reaction Steps

A solution of tert-butyl 3-phenylpiperazine-1-carboxylate (0.95 g, 3.6 mmol), benzyl chloroformate (0.85 g, 5.0 mmol) and diisopropylethylamine (1.0 g, 7.7 mmol) in dioxane (20 mL) was heated to 95° C. for 3 hours. After cooling, the reaction mixture was diluted with ethyl acetate (100 mL), and washed with saturated aqueous sodium bicarbonate (50 mL) and brine (25 mL). After drying over anhydrous sodium sulfate, filtration and concentration, the residue was purified by silica gel column chromatography (ethyl acetate/hexanes, 1:8) to give 1-benzyl 4-tert-butyl 2-phenylpiperazine-1,4-dicarboxylate (0.84 g, 59% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637499B2
Source datasetuspto-grants-2014_01
ORD IDord-80e881508e534ff1bce91a395aef24fb
Source noteuspto-grants-2014_01