Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxalic Acid | HCID 971 | — |
| Edukt | 3-Bromobenzaldehyde | HCID 76583 | — |
| Edukt | 1,2-Diaminobenzene (D4, 98%) | HCID 10772950 | — |
| Lösungsmittel | Water ethanol | HCID 19096565 | — |
| Produkt | 2-(3-Bromophenyl)benzimidazole | HCID 278822 | 26,6% |
Reaktionsschritte
Method 1—Step a O-phenylenediamine (81.8 g, 756.6 mmol) and oxalic acid (3.40 g, 37.8 mmol) were completely dissolved in EtOH—H2O/1:1 (2 L) previously warmed at 80° C. 3-Bromobenzaldehyde (44.10 mL, 378.30 mmol) was then added dropwise to the solution. The reaction mixture was stirred overnight at 70° C. to the open air. The day after solid was filtered off and triturated with MeOH (150 mL) to give the product as a pale yellow solid (27.50 g). 3.8 g were recovered from the mother liquors. Total yield 31.30 g (30%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835648B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-deb0a06724304497a43c4cc34d772a92 |
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| Quellennotiz | uspto-grants-2014_09 |
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