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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 501221Erstellt: 25. Oktober 2026

Stannous chloride dihydrate → 1-(4-Hydrazinobenzyl)-4-methylpiperazine

https://huagongshe.com/reaction/501221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStannous chloride dihydrateHCID 61436—
Edukt4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
Produkt1-(4-Hydrazinobenzyl)-4-methylpiperazineHCID 6846522299,1%

Reaktionsschritte

To a stirred solution of 4-[(4-methylpiperazin-1-yl)methyl]aniline (3.2 g, 15.57 mmol) in acetic acid: concentrated HCl (32:32 mL) at 10° C. was added NaNO2 (1.30 g, 18.78 mmol) in water (16 mL) and stirred for 10 min. Freshly prepared SnCl2.2H2O (11.75 g, 51.97 mmol) in concentrated HCl (32 mL) was added at 10° C. The temperature of the reaction mixture was allowed to rise to room temperature and maintained there for 4 hr. After filtering the reaction mixture, the precipitate was washed with water and the solid obtained was dried under reduced pressure to obtain 1-(4-hydrazinobenzyl)-4-methylpiperazine (3.4 g). 1H NMR (CD3OD, 200 MHz) δ: 7.66 (2H, d, J=8.4 Hz), 7.13 (2H, d, J=8.4 Hz), 4.46 (2H, s), 3.72 (8H, bm), 3.11 (3H, s);

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772245B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-09f2e740fd884df3b87df1985fce89cf
Quellennotizuspto-grants-2010_08