Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | p-Tolylthiourea | HCID 722833 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Amino-6-methylbenzothiazole | HCID 17335 | 67% |
Reaktionsschritte
(4-Methylphenyl)thiourea (2 mmol) was added to AcOH (4 ml), and the suspension was heated to 80° C. To the solution formed was added 33% HBr in AcOH (4 mmol) followed by DMSO (2.1 mmol). After stirring at 80° C. for 1 h, the reaction mixture was cooled to 50° C., diluted with EtOAc (10 ml) and filtered. The product (as HBr-salt) was taken up in H2O (5 ml) and treated with 1M aq. NaHCO3 (2 ml). Stirring was continued for 0.2 h. The precipitated aminobenzothiazole was then filtered, washed with H2O (10 ml) and dried (16 h at 45° C./20 mb); yield 67%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087761B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-2c38c04a2ff54f61871a1c6ab0095848 |
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| Quellennotiz | uspto-grants-2006_08 |
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