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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58168Erstellt: 26. Oktober 2026

1-Ethylpiperazine → 4-(4-Ethyl-piperazin-1-ylmethyl)-2-nitro-phenylamine

https://huagongshe.com/reaction/58168

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-EthylpiperazineHCID 79196—
EduktSodium borohydrideHCID 4311764—
Edukt4-Amino-3-nitrobenzaldehydeHCID 13237703—
KatalysatorHCID 178460666HCID 178460666—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(4-Ethyl-piperazin-1-ylmethyl)-2-nitro-phenylamineHCID 5504639534%

Reaktionsschritte

To a stirred solution of 1-ethyl-piperazine (1.37 g, 12 mmol) in MeOH (30 mL) was added Ti(OiPr)4 (1.73 g, 6 mmol). Then the solution was stirred at room temperature for 15 min. Then 4-amino-3-nitro-benzaldehyde (Procedure 2F, steps a-b, 1.5 g, 9 mmol) in MeOH (10 mL) was added and the solution was stirred at room temperature overnight. Then NaBH4 (380 mg, 10 mmol) was added and the solution was stirred at room temperature for 1 hour. The solution was diluted with EtOAc and filtered. The filtrate was washed with water and brine, dried over anhydrous Na2SO4. Concentration gave product, which was purified by flash chromatography on silica to obtain the title compound (800 mg, yield: 34%). MS (ESI): 265 [M+H]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434697B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-09b9e11eaef04abeafbfb647896bb2e2
Quellennotizuspto-grants-2016_09