Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20268170 | HCID 20268170 | — |
| Reactant | HCID 74084146 | HCID 74084146 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 74084145 | HCID 74084145 | — |
Reaction Steps
52 g of 2,5-dimethyl-benzothiazole hydrobromide and 48 g of potassium 3-hydroxy-1-propensulphonate were heated to 140° C. for 1 hour. 90 ml of acetic anhydride and 32 ml of triethylamine were added to the resulting melt of the quaternary salt and the mixture was stirred at 100° C. for 1 hour. The acetic acid formed in the reaction was then distilled off and the residue was taken up with water. Hydrochloric acid was added, whereupon the intermediate product crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04539408 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-726375ef8e7f47a0b6136eba8c058858 |
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| Source note | uspto-grants-1985_09 |
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