Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 9859173 | HCID 9859173 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23500565 | HCID 23500565 | 52% |
Reaction Steps
Potassium hydroxide (0.47 g, 8.39 mmol) was dissolved in 10 mL of 50% aqueous THF. To this was added a solution of the product of Example 4 in 6 mL THF and the reaction mixture was stirred for 2 h at 25° C. Diethylether (20 mL) was then added and the reaction mixture was made acidic by adding 10 mL of 1N HCl. The organic layer was separated, dried over magnesium sulfate, filtered and all solvent evaporated to give 0.43 g (52% yield) of the title product. The structure of the compound was characterized by 1H and 13C NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552052B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-80a41c34e8724b03a9bcccdcb8be0b89 |
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| Source note | uspto-grants-2003_04 |
|---|