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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289457Generated: October 26, 2026

(Aminomethyl)phosphonic acid → N-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acid

https://huagongshe.com/reaction/1289457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Aminomethyl)phosphonic acidHCID 14017—
Reactant2,4-Dichloro-5-nitrobenzotrifluorideHCID 621179—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acidHCID 2213222268.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

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 4N 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750525
Source datasetuspto-grants-1998_05
ORD IDord-ebb732519bdf426cb2fb74e10190ea79
Source noteuspto-grants-1998_05