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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

反応式

関与物質

役割名称HCID仕込み量
反応物(Aminomethyl)phosphonic acidHCID 14017—
反応物2,4-Dichloro-5-nitrobenzotrifluorideHCID 621179—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物N-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acidHCID 2213222268.2%

反応条件

温度120 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05955461
出典データセットuspto-grants-1999_09
ORD IDord-59297c84265743d68a9221d0db48b81b
出典メモuspto-grants-1999_09