HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328329Generated: October 30, 2026
N,N-Diisopropyl-2-benzothiazolesulfenamide → HCID 53779465, compound
https://huagongshe.com/reaction/328329
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Diisopropyl-2-benzothiazolesulfenamide | HCID 7228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53779465 | HCID 53779465 | 84.5% |
Reaction Steps
133 parts of N,N-diisopropyl-2-benzothiazolesulphenamide are suspended in 400 parts of water in an apparatus provided with a stirrer and a thermometer. 20 parts of sodium carbonate and 20 parts of sodium bicarbonate are added. 400 parts by volume of a sodium hypochlorite solution titrating 180 g. per liter of NaClO are gradually introduced in a period of 1 hour, with good stirring, at a temperature of 25°-28° C. The mixture is stirred for a further 10 hours at 20°-25° C. The solid is filtered off, washed with water until neutral and dried in vacuo. 119 parts of 2-N,N-diisopropylbenzo-thiazole-sulphinamide are obtained, that is a yield of 84.5%. Melting point (uncorrected): 79.5° C. After recrystallising from ethyl alcohol, a product of melting point (uncorrected) 80.5° C. is obtained.
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-365699c3b35146f0824d5b64b94594c7 |
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| Source note | uspto-grants-1977_04 |
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