Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22853714 | HCID 22853714 | — |
| Reactant | 5'-(t-Butyldimethylsilyl)-5-methyl-3'-deoxy-uridine | HCID 53759132 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Catalyst | HCID 131712986 | HCID 131712986 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67717591 | HCID 67717591 | 59.6% |
Reaction Steps
Chromium trioxide (7.63 g, 76.3 mmol) was added to 150 mL of dry methylene chloride containing 12.059 g (152.6 mmol) of pyridine. The mixture was stirred for 15 minutes. In a separate flask, 793 mg (19.08 mmol) of 5'-O-(t-butyldimethylsilyl)-5-methyl-3'-deoxyuridine from Step 2 was dissolved in approximately 100 mL of methylene chloride. The chromium trioxide-pyridine solution was added to the solution of 5'-(t-butyldimethylsilyl)-5-methyl-3'-deoxy-uridine and 1.946 g (19.08 mmol) of acetic anhydride was added immediately. After stirring at ambient temperature for 0.5 h, the reaction mixture was diluted with approximately 250 mL of ethyl acetate then filtered through Celite filter aid and through florisil eluted with ethyl acetate. The solvent was evaporated and the residue purified on silica gel eluted with 90% ethyl acetate in hexanes. The title compound was obtained in 59.6% yield (4.08 g), [α]D23 =+38.0° (c, 1.31, MeOH). Analysis calculated for C16H26N2O5Si: C, 54.24; H, 7.34; N, 7.91. Found: C, 54.25; H, 7.36; N, 7.88
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420276 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-0998b483507a4e7b8b4e5f96dd475c70 |
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| Source note | uspto-grants-1995_05 |
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