HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052003Generated: October 29, 2026
Ammonia → 5-(N-formyl-N-hydroxyamino)pentylphosphonic acid
https://huagongshe.com/reaction/2052003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20337183 | HCID 20337183 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(N-formyl-N-hydroxyamino)pentylphosphonic acid | HCID 20185719 | 99.5% |
Reaction Steps
Formic acid (1.19 g.) was added dropwise to acetic anhydride (1.33 g.) at ambient temperature with stirring. After the stirring was continued at the same temperature for 30 minutes, 5-(N-hydroxyamino)pentylphosphonic acid (1.83 g.) was added to the mixture. The reaction mixture was stirred at ambient temperature for an hour and 45 minutes, and then concentrated under reduced pressure to give an oily residue. The residue was dissolved in ethanol (30 ml) and to the solution was added dropwise conc. aqueous ammonia (2 ml.) to give crystals. After the mixture containing crystals was stirred at ambient temperature for an hour, the crystals were separated by filtration and dried to give crystalline monoammonium salt of 5-(N-formyl-N-hydroxyamino)pentylphosphonic acid (2.10 g.). A part (1.8 g.) of the crystals was dissolved in water (6 ml.) to give insoluble materials, which were removed by filtration and washed with water. The filtrate and the washings were combined and ethanol (30 ml.) was added thereto under heating at 60° C. to give purified crystals (1.62 g) of the same compound as mentioned above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182758 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-348ea6a4feac457ba5a68cd119471f18 |
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| Source note | uspto-grants-1980_01 |
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