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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diethyl 3-(N-Hydroxyamino)propylphosphate | HCID 9794336 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-diethoxyphosphorylpropyl)-N-hydroxy-acetamide | HCID 15434528 | 112.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680308B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-a93ccdecd09d475cb21c50fa25c12c01 |
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| Source note | uspto-grants-2004_01 |
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