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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 616560Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/616560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzoxybenzeneHCID 10316—
EduktSodium hydrosulfideHCID 28015—
EduktDiazene, bis(2,5-dichlorophenyl)-, 1-oxideHCID 14205666—
LösungsmittelMethanolHCID 887—
Produkt1,2-Bis(3-chlorophenyl)hydrazineHCID 25791976%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

85 Parts of an aqueous solution of technical sodium hydrosulfide containing 35 percent NaHS and 9 percent Na2S 2 O3 were added to a mixture comprising 65.4 parts of 2,2'-dichlor-5,5'-dichloroazoxybenzene in 196 parts of methanol at room temperature within 90 minutes. The reaction mixture was then refluxed at 70° C to75° C for a period of 5 hours. The pH had been kept between 9 and 9.4. After this period the starting azoxybenzene was shown to be all consumed and the reaction mixture was cooled down to 0° C to 5° C, and the resulting precipitate filtered off and washed with water until alkali-free. After drying below 70° C 48 parts of 2,2'-dichloro,-5,5'-dichlorohydrazobenzene of a melting point of 116° C were obtained, this representing yield of 76 percent of the theory.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04075198
Quelldatensatzuspto-grants-1978_02
ORD IDord-16d0f3124ce94af09b5ea96fa48dc704
Quellennotizuspto-grants-1978_02