Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 3-(Hydroxyamino)propylphosphonic acid | HCID 342170 | — |
| Lösungsmittel | Formic Acid | HCID 284 | — |
| Produkt | Fosmidomycin | HCID 572 | — |
| Produkt | Ethanolamine | HCID 700 | — |
Reaktionsschritte
Formic acid (1.0 ml.) was added dropwise to acetic anhydride (1.2 ml.) at ambient temperature with stirring. The stirring was continued at the same temperature for 30 minutes and then 3-(N-hydroxyamino)propylphosphonic acid (1.51 g.) was added to the mixture. The reaction mixture was stirred at ambient temperature for 1.5 hours and concentrated under reduced pressure to given an oily residue, which was dissolved in ethanol (20 ml.). To the aqueous solution was added ethanolamine (0.61 g.) to precipitate an oil, which was separated by decantation and crystallized with ethanol (20 ml.) to give crystals. The crystals were separated by filtration, washed with ethanol and dried to give crystalline monoethanolamine salt of 3-(N-formyl-N-hydroxyamino)propylphosphonic acid (1.75 g.), a part (1.5 g.) of which was recrystallized from 90% aqueous ethanol to give the purified object compound (1.15 g). M.p. 139°-142° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04182758 |
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| Quelldatensatz | uspto-grants-1980_01 |
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| ORD ID | ord-8bbfae82b73349da98f7cbfe609f6cb5 |
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| Quellennotiz | uspto-grants-1980_01 |
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