関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,6-Difluorobenzoyl isocyanate | HCID 2733369 | — |
| 反応物 | (4-Chlorophenyl)cyclopropylmethanone O-[(4-aminophenyl)methyl]oxime | HCID 54230357 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | Flucycloxuron | HCID 86309 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04550202 |
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| 出典データセット | uspto-grants-1985_10 |
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| ORD ID | ord-a5f6fd491a2445cd85b97772a6b968ac |
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| 出典メモ | uspto-grants-1985_10 |
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