Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21103259 | HCID 21103259 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10280804 | HCID 10280804 | 27.5% |
Reaction Steps
The compound of Example 59 (0.56 g, 0.99 mmol) was dissolved in 8 mL of THF, and 2 mL of 2N NaOH were added dropwise while maintaining the temperature at 0° C. After stirring at room temperature for 2 hours, 20 mL of distilled water were added and a 2N HCl solution was further added to control the pH to 1-2, and then the reactant was extracted with ethyl acetate. The supernatant was collected, and dried and concentrated under reduced pressure, and then recrystallized with ethyl acetate/hexane to obtain a light yellow solid compound (0.15 g, yield 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07223751B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-e1ff67f039b54ee0ade4997e70d335c9 |
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| Source note | uspto-grants-2007_05 |
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