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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356206Generated: November 1, 2026

Acetic Anhydride → Tert-butyl 4-acetylpiperazine-1-carboxylate

https://huagongshe.com/reaction/2356206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-acetylpiperazine-1-carboxylateHCID 2270702393%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tert-Butyl piperazine-1-carboxylate (4.00 g, 21.4 mmol) is dissolved in dichloromethane (40 mL), cooled to 0° C. and treated with acetic anhydride (2.23 mL, 23.6 mmol) over a period of 2 min. The reaction mixture is stirred at 0° C. for 30 min, LCMS analysis used to indicate completion of the reaction and the volatiles evacuated in vacuo. The residue is treated carefully with NaHCO3 (sat. aq., 50 mL), stirred vigorously for 30 min and the resulting mixture extracted with diethyl ether (4×20 mL). The combined organic extracts are dried (MgSO4), filtered and concentrated in vacuo to afford tert-Butyl-4-acetylpiperazine-1-carboxylate as a white solid (4.53 g, 93%). 1H NMR (400 MHz, DMSO-D6) δ ppm 1.39 (s, 9H), 1.99 (s, 3H), 3.22-3.29 (m, 2H), 3.30-3.34 (m, 2H), 3.36-3.41 (m, 4H); ESI-MS: m/z 229.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759339B2
Source datasetuspto-grants-2010_07
ORD IDord-8de8390b71e4411b9fae1fd36cf6be77
Source noteuspto-grants-2010_07