Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 57672422 | HCID 57672422 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25056010 | HCID 25056010 | 83.4% |
Reaction Steps
To a stirred solution of 2.2 (0.0421 g, 0.0934 mmol) in THF (2.00 mL) and EtOH (2.00 mL) at 23° C. was added 1N lithium hydroxide (2.00 mL, 2.00 mmol). Stirring continued for 16 hours. The reaction mixture was concentrated in vacuo. 1N HCl was added to reach pH 1, and the resulting mixture was extracted with EtOAc (3×10 mL), dried over MgSO4 and concentrated in vacuo. The residue was then purified by flash chromatography (SiO2 gel 60, eluted with 0%-20% EtOAc in hexanes) to give a clear oil (0.034 g, 82% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.59 (1H, d, J=8.2 Hz), 7.41 (1H, dd, J=8.6, 2.2 Hz), 7.22 (1H, dd, J=9.0, 7.4 Hz), 7.11 (1H, d, J=2.2 Hz), 7.00 (1H, t, J=8.6 Hz), 6.88-6.79 (5H, m), 5.01 (2H, s), 3.79 (3H, s), 2.94 (2H, t, J=7.8 Hz), 2.68 (2H, t, J=7.8 Hz), 1.24 (9H, s). MS ESI (neg.) m/e: 871.3 (2M−H)+, 435.1 (M−H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572934B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-10418dd77cc140f9aaccbd0f8ba41105 |
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| Source note | uspto-grants-2009_08 |
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