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HRID 618645作成日:2026年10月27日
(Aminomethyl)phosphonic acid → N-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acid
https://huagongshe.com/reaction/618645
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (Aminomethyl)phosphonic acid | HCID 14017 | — |
| 反応物 | 2,4-Dichloro-5-nitrobenzotrifluoride | HCID 621179 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acid | HCID 22132222 | 68.2% |
反応手順
3.3 g (30 mmol) of aminomethanephosphonic acid in 120 ml of water and 120 ml of ethanol are introduced together with 3.37 g (31.8 mmol) of soda and mixed with 7.8 g (97%, 30 mmol) of 3-trifluoromethyl-4,6-dichloronitrobenzene, and it is refluxed for 4 hours at 120° C. bath temperature. After removing the ethanol in a rotary evaporator, it is extracted three times with 100 ml of ethyl acetate. The organic phase is washed with a little water. It contains starting material and is discarded. The collected aqueous phase is adjusted acidic with 4 N hydrochloric acid to pH 1 and extracted three times with 100 ml of ethyl acetate each. The organic phase is washed with water, dried, filtered and concentrated by evaporation. 6.85 g (68% of theory) of N-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acid of melting point 207.3° C. is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05955461 |
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| 出典データセット | uspto-grants-1999_09 |
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| ORD ID | ord-59297c84265743d68a9221d0db48b81b |
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| 出典メモ | uspto-grants-1999_09 |
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