Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,6-Difluorobenzoyl isocyanate | HCID 2733369 | — |
| Edukt | (4-Chlorophenyl)cyclopropylmethanone O-[(4-aminophenyl)methyl]oxime | HCID 54230357 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Flucycloxuron | HCID 86309 | — |
Reaktionsschritte
36.6 g of 2,6-difluorobenzoylisocyanate in 50 ml of dry diethyl ether were added to a solution of 59.0 g 4-(α-cyclopropyl-4-chlorobenzylideneaminooxymethyl)aniline in 700 ml of dry diethylether with external cooling at 0°-10° C. After stirring for 3 hours at 0°-10° C. the formed precipitate was sucked off, washed with diethyl ether, and dried. The product obtained in a yield of 76.0 g was chromatographed over silica, chloroform being used as an eluent. The desired product was isolated in a yield of 60,7 g having a purity of at least 95% (PMR). The product obtained had a melting range of 145°-175° C. and comprised the syn- and anti-form in approximately equal amounts. In another experiment the desired product was obtained as a mixture of the syn- and anti-form in a ratio of 85:15; melting point 187°-191° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04609676 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-61489c975bce4bc38f0c43b42002ca97 |
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| Quellennotiz | uspto-grants-1986_09 |
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