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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795321Generated: October 30, 2026

Acetic Anhydride → 1-Acetyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/reaction/1795321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-4-(4-nitrophenyl)piperazineHCID 2865149—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(4-Nitrophenyl)piperazine (2.5 g, 12.1 mmol) was dissolved in dichloromethane (100 ml). Triethylamine (2.6 ml, 14.5 mmol) was added and the reaction was cooled to 0° C. Acetic anhydride (1.25 ml, 13.3 mmol) was added dropwise and the reaction was stirred at 0° C. for 1 h. Saturated sodium bicarbonate was added and the reaction was extracted (×3) with dichloromethane, dried (MgSO4), filtered and concentrated in vacuo to give 4-(4-nitrophenyl)-1-acetylpiperazine as a yellow solid (3.01 g,). GC/MS (EI, M+) m/z=249.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026314B2
Source datasetuspto-grants-2006_04
ORD IDord-2efa52dcaedc460898707ad23c0945e6
Source noteuspto-grants-2006_04