Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl tetrahydropyran-4-ylacetate | HCID 2773412 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tetrahydropyran-4-ylacetic acid | HCID 2773575 | — |
Reaction Steps
20 ml of methanol, 10 ml of water and 1 g of sodium hydroxide were added to 0.9 g of ethyl 4-tetrahydropyranylacetate and agitated at 80° C. for 1 hour. The solvent was removed by distillation, to which water was added. After washing with ethyl acetate, a hydrochloric acid aqueous solution was added to the resultant aqueous phase to an extent of pH of 3, followed by extraction with chloroform under salting-out conditions and drying with anhydrous magnesium sulfate. This was removed by filtration and the solvent was distilled off, thereby obtaining 0.87 g of a crude intended compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05382579 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-23d169cc9bf04411a9cc9427df4baff5 |
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| Source note | uspto-grants-1995_01 |
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