Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 58292829 | HCID 58292829 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58292754 | HCID 58292754 | 51.8% |
Reaction Steps
To a solution of ethyl 2-(1-hydroxy-4-isopropoxy-6-(tetrahydro-2H-pyran-2-yloxy)-1,3-dihydrobenzo[c][1,2]oxaborol-3-yl)acetate (110 mg, 0.29 mmol) in EtOH (4 mL) was added an aqueous solution of lithium hydroxide (25.2 mg, 0.60 mmol) in water (1 mL). The reaction mixture was stirred at room temperature for 30 min and acidified with 1N HCl to pH=4. The resulting mixture was extracted with EtOAc (2×20 mL). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by prep HPLC to give the title compound as a white powder (40 mg. Yield: 51.8%). 1H NMR (400 MHz, CDCl3) δ12.2 (s, 1H), 9.38 (s, 1H), 9.08 (s, 1H), 6.64 (3, 1H), 6.46 (s, 1H), 5.29-5.32 (m, 1H), 3.55 (m, 2H), 3.06-3.10 (m, 1H), 2.00-2.02 (m, 1H), 1.29-1.33 (m, 3H). MS (ESI) m/z=267 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343944B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8b9a94bc8fd14410a8b3cfd75d916399 |
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| Source note | uspto-grants-2013_01 |
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