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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Acetyl-4-(4-nitrophenyl)piperazine | HCID 2865149 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026314B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-2efa52dcaedc460898707ad23c0945e6 |
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| Source note | uspto-grants-2006_04 |
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