Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Deoxyadenosine | HCID 13730 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Sodium Pyrosulfite | HCID 656671 | — |
| Lösungsmittel | Sodium Acetate | HCID 517045 | — |
| Produkt | 8-Bromo-2'-deoxyadenosine | HCID 96547 | 64% |
Reaktionsschritte
2′-deoxyadenosine (7 gm, 25.9 mmol) was dissolved in sodium acetate buffer (150 mL, 1 M, pH 5.0) by worming it to about 50° C., then was cooled dawn to 30° C., then 3 mL of bromine in 100 mL of the same buffer was added drop wise at RT for 15 min, to the reaction. After 6 hrs the TLC on silica gel (20% MeOH in CH2Cl2) showed that all starting material was converted to a new product. The reaction was discolored by adding some sodium metabisulfite (Na2S2O5) while stirring. The color changed to a white solution, and the pH of the reaction was neutralized by adding 1 M NaOH. The reaction mixture was kept at 4° C. (refrigerator) for 16 hrs. The solid material was then filtered, washed with cold water, then acetone to give a solid yellow powder product (5.75 gm, 64%). The structure of this product was confirmed by H-NMR and ES-MS.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06916612B2 |
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| Quelldatensatz | uspto-grants-2005_07 |
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| ORD ID | ord-4c999cd990834cd0b7f8ee00b761de84 |
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| Quellennotiz | uspto-grants-2005_07 |
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