Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassiumHCID 5462222—
ReactantEthyl EthoxycarbonyloxycarbamateHCID 11446651—
Reactant1-Chloro-3-diethoxyphosphoryl-propaneHCID 13323297—
SolventDimethylformamideHCID 6228—
Productdiethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)propylphosphonateHCID 2033721390.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206156
Source datasetuspto-grants-1980_06
ORD IDord-3c9035176e104eee9d3c7f23936fa107
Source noteuspto-grants-1980_06