Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Fluorophenyl isocyanate | HCID 70955 | — |
| Edukt | Thiobarbituric acid | HCID 2723628 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 20223045 | HCID 20223045 | — |
Reaktionsschritte
2-thiobarbituric acid (14.4 g) was suspended in pyridine and 4-fluorophenyl isocyanate (13.7 g) was added thereto. The reaction mixture was maintained at 90° C. for one hour, and thereafter left overnight at room temperature. The solids formed were collected, washed with pyridine, re-suspended in ethanol, and again collected and dried. A pale pink powder product was thereby obtained, mp >250° C. (dec.), NMR (DMSO) 7.0-7.7δ (multiplet, integral 4); 10.7-11.4δ (overlapping broad singlets, combined integral 4). MS, M/e 281 (Calc., 281).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04634707 |
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| Quelldatensatz | uspto-grants-1987_01 |
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| ORD ID | ord-8411a693a2244562bb1b98915c09dac2 |
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| Quellennotiz | uspto-grants-1987_01 |
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