Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 6-Chloro-2,4-dinitroaniline | HCID 19052 | — |
| Edukt | Selenium | HCID 6326970 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Chloro-6-aminobenzimidazolone | HCID 18970469 | 84% |
Reaktionsschritte
2,4-Dinitro-6-chloroaniline 2.7 g (12.5 m moles), selenium 1.98 g (25.0 m moles), water 1.6 ml (89 m moles), triethylamine 5.0 g (50 m moles) and tetrahydrofuran 100 ml were placed in a 200-ml capacity autoclave, and stirred at a temperature of 80° C. for five hours under carbon monoxide of 20 Kg/cm2. The reaction mixture obtained was worked up in the same manner as in EXAMPLE 1, to provide 4-chloro-6 -aminobenzimidazolone in 84% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04393216 |
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| Quelldatensatz | uspto-grants-1983_07 |
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| ORD ID | ord-e5adb9b5df6e4e2b89c34407576fa6c0 |
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| Quellennotiz | uspto-grants-1983_07 |
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