HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284597Generated: October 30, 2026
Sulfuryl chloride → 6-Chloro-2-benzothiazolamine
https://huagongshe.com/reaction/1284597
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Thourea, (4-chlorophenyl)- (9CI) | HCID 735843 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 6-Chloro-2-benzothiazolamine | HCID 7226 | 85% |
Reaction Steps
186.5 parts of 4-chlorophenylthiourea were suspended with stirring in 850 parts of chlorobenzene, and 185 parts of sulfuryl chloride were added uniformly with stirring at a temperature of 40°-45° C. within about 3 hours. After the immediately starting gas development had ceased, the suspension formed which could be stirred with difficulty only was liberated from the chlorobenzene by steam distillation. The remaining suspension of 2-amino-6-chlorobenzothiazolium chloride was adjusted to pH 8 with 25% ammonia solution, thus causing the crude 2-amino-6-chlorobenzothiazole to agglomerate to a tacky mass. By decantation and drying, 146.3 parts of 2-amino-6-chlorobenzothiazole containing about 85% of pure product were obtained (=124.4 parts of 100% product, 67.4% of th.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04563533 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-f5846bc2010e4544b29535946ac5f83e |
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| Source note | uspto-grants-1986_01 |
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