Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66599153 | HCID 66599153 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66598088 | HCID 66598088 | 47% |
Reaction Steps
Under an argon atmosphere, 2,3-dihydro-[1,4]dioxino[2,3-b]pyridine-6-carbonitrile (16 mg, 99 μmol) was dissolved in tetrahydrofuran (500 μL), added methyllithium (150 μL (1.04 M in THF solution), 148 μmol) under ice-cold conditions, and the mixture was stirred at the same temperature for 5 minutes. The reaction solution was added 1M-sulfuric acid (2.0 mL), and stirred at room temperature for 3 hours. Under ice-cold conditions, the reaction solution was added a saturated aqueous solution of sodium hydrogen carbonate (pH=8 was confirmed). The reaction solution was extracted with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was purified by silica-gel column chromatography (hexane/ethyl acetate), and the title compound (8.3 mg (yield 47%)) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551985B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-46805f99510346e49d41c84f9799f2c5 |
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| Source note | uspto-grants-2013_10 |
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