HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706180Generated: November 1, 2026
Potassium → diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)propylphosphonate
https://huagongshe.com/reaction/1706180
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Ethyl Ethoxycarbonyloxycarbamate | HCID 11446651 | — |
| Reactant | 1-Chloro-3-diethoxyphosphoryl-propane | HCID 13323297 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)propylphosphonate | HCID 20337213 | 90.3% |
Reaction Steps
To a solution of diethyl 3-chloropropylphosphonate (430.6 g) in dry N,N-dimethylformamide (2.25 l) was added potassium salt of ethyl N-ethoxycarbonyloxycarbamate (429.2 g). This mixture was stirred at 64°-66° C. for three hours. After the resulting potassium chloride was removed by filtration, the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (2.0 l) and washed with water (4.0 l). The aqueous layer was extracted twice with ethyl acetate (1.2 and 0.8 l). The combined ethyl acetate layer was washed with saturated aqueous sodium chloride solution (1.5 l), dried over magnesium sulfate and concentrated under reduced pressure to give oily diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)-propylphosphonate (643.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04206156 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-3c9035176e104eee9d3c7f23936fa107 |
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| Source note | uspto-grants-1980_06 |
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