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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840259Generated: October 31, 2026

Acetic Anhydride → N-(3-diethoxyphosphorylpropyl)-N-hydroxy-acetamide

https://huagongshe.com/reaction/1840259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiethyl 3-(N-Hydroxyamino)propylphosphateHCID 9794336—
SolventDichloromethaneHCID 6344—
ProductN-(3-diethoxyphosphorylpropyl)-N-hydroxy-acetamideHCID 15434528112.4%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

2.8 g (0.013 mol) 3-(N-hydroxyamino)-propylphosphonic acid diethylester are dissolved in 30 ml methylene chloride and added drop by drop with cooling with ice to 2.65 g (0.026 mol) acetic anhydride. The reaction mixture is stirred for 30 minutes at 0-5° C. and for a further 1.5 hours at room temperature. After concentration under reduced pressure until a yellow oily radical is achieved, this oily residue is taken up in 15 ml methanol and 5 ml water, adjusted to pH 8 with 2 n NaOH and stirred for a further 1.5 hours at room temperature. Methanol is removed under reduced pressure and the resultant solution is adjusted to pH=5 with concentrated HCl. The yellow solution is extracted repeatedly with methylene chloride (1×30 ml, 2×10 ml in each case), the combined CH2Cl2 phases are dried over MGSO4 and the solvent is removed at room temperature under reduced pressure. 3.7 g of a yellow oil are obtained which are freed from adhering volatile substances in the entire diaphragm pump vacuum. 2.78 g yellow oil remain.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680308B1
Source datasetuspto-grants-2004_01
ORD IDord-a93ccdecd09d475cb21c50fa25c12c01
Source noteuspto-grants-2004_01