Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856628Generated: October 26, 2026

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

https://huagongshe.com/reaction/1856628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(Aminomethyl)phosphonic acidHCID 14017—
Reactant2,4-Dichloro-5-nitrobenzotrifluorideHCID 621179—
SolventAcetonitrileHCID 6342—
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 is introduced into 120 ml of water and 120 ml of acetonitrile 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 refluxed for 4 hours at a bath temperature of 120° C. After the acetonitrile is drawn off 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 made acidic at pH 1 with 4N hydrochloric acid 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 with a melting point of 207.3° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143733
Source datasetuspto-grants-2000_11
ORD IDord-7e94b2c4f93e4fdb83fa452f7d78d6d8
Source noteuspto-grants-2000_11