Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | Diazene, bis(2-methoxyphenyl)-, 1-oxide | HCID 353717 | — |
| Product | HCID 86735484 | HCID 86735484 | 72% |
Reaction Steps
90 parts of an aqueous solution of technical sodium hydrosulfide containing 35 percent NaHS and 4 percent NasS2O3 were added to a mixture comprising 51.6 parts of 2,2'-dimethoxyazoxybenzene in 155 parts methanol at room temperature within 5 hours. Subsequently, the reaction mixture was refluxed at 70° C to 75° C for 2 1/2 hours while the pH was maintained between 8.5 and 9.4. After this period the absence of the starting material was confirmed and the reaction mixture was cooled down to 0° C to 5° C, the reduced product that precipitated filtered off and washed with water until alkali-free. After drying below 70° C, 35 parts of 2,2'-dimethoxyhydrazobenzene of a melting point of 100° C to 102° C were obtained, this representing a commercially acceptible grade in a yield of 72 percent of 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-4d0ecd5f839e43cd90baa059658b848a |
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| Source note | uspto-grants-1978_02 |
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