関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 4-Chloro-2-nitroaniline | HCID 6979 | — |
| 反応物 | Diethoxymethane | HCID 10024 | — |
| 反応物 | Diethylphosphite | HCID 3780918 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Diethyl (4-chloro-2-nitroanilino)methylphosphonate | HCID 603785 | 95% |
反応手順
With stirring and under a nitrogen atmosphere 4-chloro-2-nitroaniline (5 g, 28.9 mmole) was dissolved in diethylphosphite (21.44 g, 155 mmole), followed by the addition of a solution of sulfuric acid (0.1 mL) and water (0.1 mL). Under a continuous flow of nitrogen the solution was heated to 95° C., after which diethoxymethane (9.05 g, 86.8 mmole) was added in a dropwise manner over a period of 1.5 hours while maintaining the temperature between 93°-97° C. Once all the diethoxymethane was added, the reaction was kept at 95°-105° C. for another hour after which the mixture was cooled to 45°-50° C. and cold water (70 mL) was added over 20 minutes. The resulting suspension was filtered, washed first with water (10 mL), then with heptane (10 mL). The obtained orange solid was dried at 30°-40° C. for 16 hours to yield 8.85 g (95%) of the title compound, mp 94°-5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05864040 |
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| 出典データセット | uspto-grants-1999_01 |
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| ORD ID | ord-aae98600148745eb81ca288f533f5fc3 |
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| 出典メモ | uspto-grants-1999_01 |
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