HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615355Generated: October 30, 2026
Sodium Hydroxide → 2-BENZOTHIAZOLESULFONAMIDE, 6-NITRO-
https://huagongshe.com/reaction/615355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | HCID 178418579 | HCID 178418579 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-BENZOTHIAZOLESULFONAMIDE, 6-NITRO- | HCID 13393427 | — |
Reaction Steps
To ammonium hydroxide (14.8M) (90 ml.) were added dropwise simultaneously sodium hypochlorite solution (5.25%) (42.4 ml.) and a solution of sodium hydroxide (1.2 g., 0.03 mole) and 2-mercapto-6-nitrobenzothiazole (6.37 g., 0.03 mole) in H2O (80 ml.) with stirring at <5° C. After 1/2 hr. the precipitated solid was collected by suction filtration and washed well with ice-H2O. The wet solid was suspended in acetone (120 ml.) with stirring at 25° C., treated with glacial acetic acid (2.4 ml.), then immediately treated dropwise wth 5% aqueous potassium permanganate solution (6.6 g, 0.04 mole in 120 ml H2O) over a 1/2 hr. period maintaining the reaction mixture temperature at <30° C. After stirring for an additional hour, the mixture was filtered to remove precipitated manganese dioxide, and the filtrate concentrated to remove the acetone and precipitate the solid product. Crystallization from 1,2-dichloroethane gave 1.18 g 6-nitro-2-benzothiazolesulfonamide, m.p. 176°-178° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04499103 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-5aa57f890ba6420faa539552c3755d5e |
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| Source note | uspto-grants-1985_02 |
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