Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 19350833 | HCID 19350833 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 19350804 | HCID 19350804 | 80% |
Reaction Steps
2-Methoxy-5-hydroxymethyltetrahydropyran (0.91 g) was dissolved in pyridine (10 ml), and the solution cooled to 5° C. Acetic anhydride (3.15 ml) was added thereto, and the mixture stirred at the same temperature For 1 hour, and then at room temperature overnight. After removing pyridine by evaporation under reduced pressure, the residue was purified on a silica gel column (eluent: n-hexane/ethyl acetate=1/2) to obtain the desired product (0.93 g, 80.0%) as pale yellow oil.
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-349b620d26544668852245794ddd7cbc |
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| Source note | uspto-grants-2000_03 |
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