Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 58292665 | HCID 58292665 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58292628 | HCID 58292628 | 23% |
Reaction Steps
To a solution of ethyl 2-(4-(benzyloxy)-1,6-dihydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-3-yl)acetate (195 mg, 0.57 mmol) in EtOH (4 mL) was added dropwise an aqueous solution of lithium hydroxide (47.9 mg, 1.14 mmol) in water (4 mL). The reaction mixture was stirred at room temperature overnight and acidified with 1N HCl to pH=3. The resulting mixture was extracted with EtOAc (2×20 mL). 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 (41.2 mg, Yield: 23%). 1H NMR (400 MHz, CDCl3) δ 9.46 (s, 1H), 9.14 (s, 1H), 7.44-7.33 (m, 5H), 6.66 (d, J=1.2 Hz, 1H), 6.54 (s, 1H), 5.36 (m, 1H), 5.12 (s, 2H), 3.15 (m, 1H), 2.07 (m, 1H). MS (ESI) m/z=315 [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-92ec3b61640f4da49b5a17675a84c27c |
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| Source note | uspto-grants-2013_01 |
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