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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (Aminomethyl)phosphonic acid | HCID 14017 | — |
| Reactant | 2,4-Dichloro-5-nitrobenzotrifluoride | HCID 621179 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-nitro-4-trifluoromethyl-5-chloro-phenyl)-aminomethanephosphonic acid | HCID 22132222 | 68.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143733 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-7e94b2c4f93e4fdb83fa452f7d78d6d8 |
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| Source note | uspto-grants-2000_11 |
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