Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | 6-Bromo-2,3-dihydro-1,3-benzothiazol-2-one | HCID 188444 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 6-Bromo-2-chlorobenzothiazole | HCID 2049871 | 95,4% |
Reaktionsschritte
DMF (0.807 mL, 10.4 mmol) was added to phosphorous oxychloride (8.10 mL, 86.9 mmol), and the reaction mixture was stirred for 15 min. 6-bromobenzo[d]thiazol-2(3H)-one (2.00 g, 8.69 mmol) was added and the reaction mixture was heated to 100° C. overnight. Upon cooling to rt, the reaction mixture was slowly added to a solution of K2CO3 (75 g) in water (200 mL) while maintaining the temperature below 35° C. Additional K2CO3 was added in order to maintain the pH above 10. Upon complete addition, the mixture was allowed to stir for 1 h. The solid was collected by filtration, washed with water (2×25 mL), and air dried. Further drying in a vacuum oven gave 2.06 g (95%) of the desired product as a brown solid. The material was used without further purification. LC-MS: RT=9.94 min., compound does not ionize.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822472B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-0cbfa0965f994ce7b31dbfe2762142bb |
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| Quellennotiz | uspto-grants-2014_09 |
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