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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885855Generated: October 26, 2026

Di-tert-butyl dicarbonate → Tert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/885855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantPiperazin-4-ylacetophenoneHCID 97269—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylateHCID 2113619091.8%

Reaction Steps

A mixture of 1-(4-piperazin-1-yl-phenyl)-ethanone (513 mg, 2.51 mmol), BOC2O (820 mg, 3.76 mmol) and TEA (0.698 ml, 5.02 mmol) in DCM (20 ml) was stirred at room temperature overnight. The resulting solution was concentrated in vacuo and then partitioned between water and AcOEt. The organic phase was dried over Na2SO4, evaporated in vacuo and the crude reaction mixture was purified by column chromatography (eluent: petroleum ether/AcOEt) to give 701 mg of 4-(4-acetyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242175B2
Source datasetuspto-grants-2012_08
ORD IDord-322c425e730140db890cb8ed1bd5e8c2
Source noteuspto-grants-2012_08