Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | N-[4-(Butane-1-sulfonyl)phenyl]ethanimidic acid | HCID 237535 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19819855 | HCID 19819855 | 70% |
Reaction Steps
255 g of p-butylsulphonylacetanilide, in a mixture of 1.5 l of water and 300 ml of concentrated hydrochloric acid, are boiled for 1 hour under reflux. After cooling to 0° C, the product is diazotised with a solution of 70 g of NaNO2 in 175 ml of water. The filtered diazonium salt solution is added, at 5°-10° C, to a mixture of 750 g of 40% strength sodium sulphite solution and 750 ml of water which had been adjusted to pH 7 with concentrated sodium hydroxide solution, the pH being maintained at 6-7 by means of concentrated sodium hydroxide solution. After standing overnight, 300 ml of concentrated hydrochloric acid are added and the mixture is boiled for 1 hour. p-Butylsulphonylphenylhydrazine of melting point 138° C (from ethanol) is obtained, in a yield of approx. 70- 75% of theory, from the cooled solution by careful addition of alkali.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04071466 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-abc88074ae2f4e0bbd6cbe2d758bc98c |
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| Source note | uspto-grants-1978_01 |
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