Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 57705500 | HCID 57705500 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57705619 | HCID 57705619 | 69.4% |
Reaction Steps
To a cooled solution of 67.20B (0.4401 g, 1.282 mmol) in dry THF (8 mL) at 0° C. was added borane THF complex, 1.0 M in THF (2.5 mL, 2.5 mmol) dropwise. Upon complete addition, the reaction was maintained at 0° C. and monitored by TLC and LCMS. After 3 hours, water was added to quench the reaction, and the resulting solution was extracted three times with EtOAc. The organic extractions were combined and washed successively with saturated aqueous sodium bicarbonate, water, and then brine. After drying over anhydrous magnesium sulfate, filtration, and concentration, the residue was purified with silica gel flash chromatography (0-25% MeOH in DCM) to afford 67.20C as an oil (292.9 mg, 69% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.85 (2H, m), 7.36 (1H, d, J=7.8 Hz), 7.11 (2H, m), 6.86 (1H, dt, J=8.9, 3.6 Hz), 3.83 (3H, s), 2.85 (4H, m), 1.46 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-2b647afeb0ea46728691b576d7c24a44 |
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| Source note | uspto-grants-2011_10 |
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