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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706232Generated: October 25, 2026

Fosmidomycin → 3-(N-benzoyloxy-N-formylamino)propylphosphonic acid

https://huagongshe.com/reaction/1706232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFosmidomycinHCID 572—
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-(N-benzoyloxy-N-formylamino)propylphosphonic acidHCID 2033722448.2%

Reaction Steps

A solution of benzoyl chloride (700 mg) in dry acetone (6 ml) was added dropwise to a solution of sodium salt of 3-(N-formyl-N-hydroxyamino)propylphosphonic acid (820 mg) in a mixture of water (15 ml) and acetone (15 ml) under ice-cooling, while stirring. During this period, pH of the mixture was kept at around 7.5-7.7 with 1 N aqueous sodium hydroxide solution. The stirring was continued at the same temperature for 10 minutes and then acetone was evaporated under reduced pressure. The resulting aqueous solution was adjusted to pH 3.5 with 1N hydrochloric acid and ether (40 ml) was added thereto. After removal of the precipitated impurities, the aqueous layer was adjusted to pH 1.6 with 1N hydrochloric acid and extracted three times with ethyl acetate (50 ml, 20 ml×2). The combined ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and evaporated to dryness to give crystals, which were washed with ether to give crystalline 3-(N-benzoyloxy-N-formylamino)propylphosphonic acid (620 mg). Mp 149°-153° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206156
Source datasetuspto-grants-1980_06
ORD IDord-430cd1d575fa4a45a8f3c406116ad0ac
Source noteuspto-grants-1980_06