Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Erythromycin | HCID 12560 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Methanol--water (1/1) | HCID 22242641 | — |
| Produkt | N-Demethylerythromycin A | HCID 10010092 | — |
Reaktionsschritte
20 g of erythromycin A (=27.2 mmole) and 11.2 g (=136.2 mmole) of sodium acetate were dissolved in 200 ml of an 8:2 methanol/water mixture. The solution was heated to 47° C. Then 6.9 g (=136.2 mmole) of iodine were added. The pH was kept at 8 to 9 by adding dilute aqueous sodium hydroxide solution. After 3 hours, the reaction mixture was worked up by pouring it into a mixture of 1 liter of water and 20 ml of ammonium hydroxide solution. The reaction mixture was extracted with ethyl acetate, and the organic extract was washed with ammonium hydroxide-containing water and concentrated. The crude product remaining after removal of the solvent was recrystallized from acetone/ammonium hydroxide solution 50:3. Melting point 143°-148° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05418224 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-4935058f3f6846f28c07983f21d3e3ee |
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| Quellennotiz | uspto-grants-1995_05 |
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