HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328327Generated: October 30, 2026
Sodium Carbonate → 2-Benzothiazolesulfinamide, N,N-dimethyl-
https://huagongshe.com/reaction/328327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hypochlorite | HCID 61739 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 14345394 | HCID 14345394 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Benzothiazolesulfinamide, N,N-dimethyl- | HCID 117983 | 90% |
Reaction Steps
10 parts of sodium carbonate and 4 parts of sodium bicarbonate are added to a well stirred suspension of 63 parts 2-N,N-dimethylbenzothiazole-sulphenamide in 130 parts of water. 170 parts by volume of a solution of sodium hypochlorite titrating 177 g. of NaClO and 3 g. of free caustic soda per liter are then slowly introduced, in about 5 hours and keeping the temperature within the range from 25° C. to below 30° C. The excess of hypochlorite is controlled by starchiodide paper. After introduction, the mixture is stirred for a further hour. The creamy white precipitate obtained is filtered off, washed until the washings are neutral and dried at 60° C. The 2-N,N-dimethyl-benzothiazole-sulphinamide melting at 121°-122° C., free from dibenzothiazyl disulphide, is obtained with a yield of 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04017506 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-15281c2d5e584f65b435eb678d0fefec |
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| Source note | uspto-grants-1977_04 |
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