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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132913Erstellt: 25. Oktober 2026

Dichloromethane → 1-(2-Chloro-6-nitrophenyl)piperazine

https://huagongshe.com/reaction/132913

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1-Boc-4-(2-chloro-6-nitrophenyl)piperazineHCID 58767704—
LösungsmittelTrifluoroacetic acidHCID 6422—
Produkt1-(2-Chloro-6-nitrophenyl)piperazineHCID 277140895,3%

Reaktionsschritte

4-(2-Chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (1.87 g, 5.47 mmol) was dissolved in trifluoroacetic acid (5.0 mL) and CH2Cl2 (5.0 mL) and allowed to stir for 2 h. The reaction mixture was concentrated, diluted with EtOAc, and washed with saturated aq. NaHCO3. The organic layer was dried over Na2SO4, concentrated and purified by column chromatography (silica, 100% CH2Cl2) to afford 1-(2-chloro-6-nitro-phenyl)-piperazine (1.26 g, 95%). MS (electrospray): exact mass calculated for C10H12CIN3O2, 241.1; m/z found, 242.1 [M+H]+. 1H NMR (400 MHz, CDCl3): 7.54 (dd, J=8.2, 1.6 Hz, 1H), 7.49 (dd, J=8.2, 1.6 Hz, 1H), 7.10 (t, J=8.2 Hz, 1H), 3.08 (br s, 4H), 2.99 (br s, 4H), 2.07-2.12 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388011B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-e9f59b15480346b1b3393c5cdd16d34b
Quellennotizuspto-grants-2008_06