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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051970Generated: November 3, 2026

Potassium → diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)propylphosphonate

https://huagongshe.com/reaction/2051970

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-dimethyformamide (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 numberUS04182758
Source datasetuspto-grants-1980_01
ORD IDord-eceaead44d384a72bfa3c08dc4acdc4b
Source noteuspto-grants-1980_01