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Diphenyl Ether → Methyl-5-(2-chloro-4-cyano-6-fluoro-phenoxy)-2-nitro-benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diphenyl Ether | HCID 7583 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | Methyl 5-hydroxy-2-nitrobenzoate | HCID 12922678 | — |
| 反応物 | 3-Chloro-4,5-difluorobenzonitrile | HCID 13643470 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | Methyl-5-(2-chloro-4-cyano-6-fluoro-phenoxy)-2-nitro-benzoate | HCID 23035893 | — |
反応手順
The product 3-chloro-4,5-difluorobenzonitrile, prepared for example as set forth in Example 3, above, is a useful intermediate for the preparation of various end products especially for the preparation of diphenyl ether herbicides. Thus, for example, this compound may be further reacted with the potassium salt of methyl-5-hydroxy-2-nitrobenzoate in a solvent, such as N-methyl-2-pyrrolidone at a temperature of about 120° to 180° Celsius to form methyl-5-(2-chloro-4-cyano-6-fluoro-phenoxy)-2-nitro-benzoate. The ester may be hydrolyzed in a conventional manner to the corresponding carboxylic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04590315 |
| 出典データセット | uspto-grants-1986_05 |
| ORD ID | ord-9654b819cb6344e78c270f6b659d72c2 |
| 出典メモ | uspto-grants-1986_05 |