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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 501219Erstellt: 25. Oktober 2026

4-Nitrobenzaldehyde → 1-Methyl-4-(4-nitrobenzyl)piperazine

https://huagongshe.com/reaction/501219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzaldehydeHCID 541—
Edukt1-MethylpiperazineHCID 53167—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Methyl-4-(4-nitrobenzyl)piperazineHCID 677795—

Reaktionsschritte

To a 0° C. cooled solution of 4-nitrobenzaldehyde in DCM (40 mL) was added Na(OAc)3BH (10.526 gm, 49.66 mmol) and the reacton was stirred for 10 min. To the reaction mixture was added N-methylpiperazine (9.93 g, 99.3 mmol) under nitrogen atmosphere and the reaction mixture was continued stirring at room temperature for 4 h. The progress of the reaction was monitored by TLC and upon completion of the reaction, the mixture was partitioned between DCM (20 mL) and water (15 mL) and the organic layer was separated, washed with water (2×15 mL), dried over sodium sulphate, filtered and the solvent was removed under reduced pressure to give crude residue. Washing with ether gave 1-methyl-4-(4-nitrobenzyl)piperazine (4 g). 1H NMR (CDCl3, 200 MHz) δ: 8.19 (2H, d, J=8.4 Hz), 7.53 (2H, d, J=8.4 Hz), 3.59 (2H, s), 2.47 (8H, bm), 2.29 (3H, s); m/e=236 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772245B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-f09d761aca3640698a4ac7c12f7da2a3
Quellennotizuspto-grants-2010_08