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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052017Generated: October 26, 2026

Hydrochloric Acid → 3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acid

https://huagongshe.com/reaction/2052017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFosmidomycinHCID 572—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantSodiumHCID 5360545—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
Product3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acidHCID 2033722775.3%

Reaction Steps

Monosodium salt of 3-(N-formyl-N-hydroxyamino)propylphosphonic acid (2.05 g.) was dissolved in a mixture of 1 N aqueous sodium hydroxide solution (20 ml.), water (10 ml.) and acetone (10 ml.). To the solution was added dropwise a solution of p-chlorobenzoyl chloride (2.10 g.) in dry acetone (5 ml.) at 0°-5° C. with stirring. After the stirring was continued at the same temperature for 30 minutes, ethyl acetate (40 ml.) was added to the reaction mixture and then the resultant mixture was adjusted to pH 1 with 10% hydrochloric acid. The ethyl acetate layer was separated and then the aqueous layer was extracted again with ethyl acetate (20 ml.). The combined ethyl acetate layer was washed with aqueous sodium chloride solution, dried over magnesium sulfate and concentrated under reduced pressure to give an oily residue, which was crystallized with ethylether (40 ml.) to give crystals. The crystals were separated by filtration, washed twice with ethylether (10 ml.) to give crystalline 3-[N-(p-chlorobenzoyloxy)-N-formylamino] propylphosphonic acid (2.71 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182758
Source datasetuspto-grants-1980_01
ORD IDord-14da13d93de2418b9ef8e4a476e5df7d
Source noteuspto-grants-1980_01