関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | 4,5-Dichloro-2-phenyl-3(2H)-pyridazinone | HCID 72813 | — |
| 生成物 | Chloridazon | HCID 15546 | — |
| 生成物 | 4-amino-5-chloro-2-phenylpyridazin-3(2H)-one | HCID 613445 | — |
反応手順
4-Chloro-5-amino-2-phenyl-3(2H)-pyridazinone is prepared from 4,5-dichloro-2-phenyl-3(2H)-pyridazinone and ammonia in high yield and substantially free from 4-amino-5-chloro-2-phenyl-3(2 H)-pyridazinone in a method comprising reacting 4,5-dichloro-2-phenyl-3(2H)-pyridazinone with aqueous ammonia in the presence of a catalyst which is capable of selectively exchanging the 5-chlorine atom in 4,5-dichloro-2-phenyl-3(2H)-pyridazinone with a leaving group of such a nature that the resulting intermediate compound is capable of alkylating ammonia to 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone in high yield in the reaction medium, thereby regenerating the catalyst. The end product is isolated by filtration after the reaction and washed with water, and the mother liquor plus the wash water are used as reaction medium for the next batch.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04454318 |
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| 出典データセット | uspto-grants-1984_06 |
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| ORD ID | ord-a5fca18204164b0eb29c6c20be24f708 |
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| 出典メモ | uspto-grants-1984_06 |
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