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 | — |
Reaktionsschritte
2′-Deoxyadenosine (7 gm. 25.9 mmol) was dissolved in sodium acetate buffer (150, 1 M, pH5.0) 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 dropwise 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 it was stirring, the color changed to a white solution, the pH of the reaction was neutralized by adding NaOH (1M solution). The reaction mixture was kept at 4° C. (refrigerator) for 16 hrs. Next day the solid material was 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 | US07771929B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-139d759e39ce42ffbc1e82e600865e5f |
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| Quellennotiz | uspto-grants-2010_08 |
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