Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Nitrosylsulfuric acid | HCID 82157 | — |
| Edukt | Phosphinic Acid | HCID 4124402 | — |
| Edukt | 7-Bromo-5-nitrobenzo[d]thiazol-6-amine | HCID 22728034 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | 7-Bromo-5-nitrobenzothiazole | HCID 22728031 | 89% |
Reaktionsschritte
To a solution of 5-nitro-6-amino-7-bromobenzothiazole (1.0 g, 3.7 mmol) in 4 mL of sulfuric acid was added nitrososulfuric acid (1.2 g, 9.5 mmol) in a portion. The resulting reaction mixture was stirred for 12 h at 25° C. The reaction mixture was then cooled to 0° C. and 1 mL of H3PO2 was added into the solution. It was stirred for 12 h at another 25° C. and for 2 h at 50° C. The reaction mixture was then poured into EtOAc and washed with aq. NaHCO3. Organic layer was dried over Na2SO4 and concentrated in vacuo to provide an oil (0.85 g, 3.2 mmol, 89%), which was characterized as the desired product(>95% pure) and subjected to a following reaction without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06303643B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-c3011ab581014581b8ca55f3bfe37049 |
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| Quellennotiz | uspto-grants-2001_10 |
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