Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 19350843 | HCID 19350843 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 19350797 | HCID 19350797 | — |
Reaction Steps
5-Benzyloxymethyl-1,4-oxathian-2-ol (3.46 g) was dissolved in pyridine (37 ml), and the solution was cooled to 5° C. Acetic anhydride (3.27 ml) was added dropwise thereto, and the solution was stirred at the same temperature for 4 hours to complete the reaction. After removing the solvent by evaporation under reduced pressure, the residue was azeotroped with toluene to completely remove pyridine to obtain pale brown syrup. The syrup was purified on a silica gel column (eluent: n-hexane/ethyl acetate=3/1) to provide the desired product (2.94 g) as colorless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06034087 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-746ae9b69e764118943eb7244c635a6e |
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| Source note | uspto-grants-2000_03 |
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