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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266676Erstellt: 26. Oktober 2026

Water → 1,2-Bis(3-chlorophenyl)hydrazine

https://huagongshe.com/reaction/266676

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Chloro-3-nitrobenzeneHCID 8489—
EduktSodium HydroxideHCID 14798—
KatalysatorZincHCID 23994—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1,2-Bis(3-chlorophenyl)hydrazineHCID 25791968,5%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a stirred solution of 50% NaOH (3 mL) was added 3-chloronitrobenzene (10 g, 64 mM). The suspension was warmed to 60° C. and zinc (9 g, 138 mM) was added. During the addition, the temperature of the reaction mixture was kept between 60° and 80° C. After the addition was complete, a solution of 20% NaOH (18 mL, 90 mM) was added followed by water (30 mL). An additional portion of zinc (12 g, 189 mM) was then added and the resulting mixture was stirred between 75°-80° C. for 2 hours. After cooling to room temperature, the mixture was added to ether (200 mL), stirred, and the liquid was decanted. The solids were then resuspended in ether and the extraction was repeated 3 times. The ether extracts were combined, dried (Na2SO4), and concentrated to give a yellow solid. This was purified by flash column chromatography using CH2Cl2 as elutant which afforded the titled compound as a yellow solid (5.5 g, 68%). NMR (CDCl3): 7.12 (t, J=8 Hz, 2H), 6.80 (m, 4H), 6.67 (dd, J1 =1 Hz, J2 =8 Hz, 2H), 5.66 (br s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05652239
Quelldatensatzuspto-grants-1997_07
ORD IDord-849d6f9dce954ca088376be8c11a50e5
Quellennotizuspto-grants-1997_07