HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616560Generated: October 26, 2026
Azoxybenzene → 1,2-Bis(3-chlorophenyl)hydrazine
https://huagongshe.com/reaction/616560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azoxybenzene | HCID 10316 | — |
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | Diazene, bis(2,5-dichlorophenyl)-, 1-oxide | HCID 14205666 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,2-Bis(3-chlorophenyl)hydrazine | HCID 257919 | 76% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04075198 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-16d0f3124ce94af09b5ea96fa48dc704 |
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| Source note | uspto-grants-1978_02 |
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