Reaktion #51517
ord-30d4dc67ffcc47cfbdd9fa717f792f80
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigeover 10 minutes
- 2workup.WAITleft
- 3workup.WAITto stand for 8 hours
- 4Sonstigeto give a gum
- 5SonstigeThe solvent was decanted
- 6Sonstigeevaporated in vacuo
- 7Sonstigeto afford a white solid which
- 8Extraktionthis solution was gently extracted with the CH2Cl2 containing the product
- 9SonstigeThe organic layer was separated
- 10Extraktionthe aqueous layer was extracted again with CH2Cl2 (2×50 mL)
- 11Trocknenthe solvent was dried over MgSO4
- 12Sonstigeevaporated in vacuo
- 13Sonstigeto afford a white foam
- 14Sonstigepurified by flash chromatography
Vorschrift
1-[2′-O-(2-Ethylacetyl)-3′,5′-bis-O-(2,4-dichlorobenzyl)-β-D-ribofuranosyl]thymine (9.92 g, 15.0 mmol) was dissolved in hot EtOH (150 mL) and the solution was cooled to ambient temperature in a water bath. To the solution was cautiously added NaBH4 (1.13 g, 30.0 mmol) over 10 minutes. After 3 hours additional NaBH4 (282 mg, 7.45 mmol) was added the mixture was stirred for 1 hour and left to stand for 8 hours. The pH was adjusted to 4 by addition of Saturated NH4Cl (25 mL) to give a gum. The solvent was decanted and evaporated in vacuo to afford a white solid which was dissolved in CH2Cl2 (250 mL). The gum was dissolved with saturated aqueous NaHCO3 and this solution was gently extracted with the CH2Cl2 containing the product. The organic layer was separated and the aqueous layer was extracted again with CH2Cl2 (2×50 mL). After combining the organic layers, the solvent was dried over MgSO4 and evaporated in vacuo to afford a white foam. The foam was dissolved in CH2Cl2 and purified by flash chromatography using hexanes-EtOAc, 20:80, to give the title compound as a white foam (8.39 g, 90%).