Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 619147 | HCID 619147 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 50900629 | HCID 50900629 | 100% |
Reaction Steps
Compound 1 (1.25 g, 5 mmol) was stirred at room temperature in acetone (16 mL). To this, KOH (1.23 g, 22 mmol) was added. The mixture stirred at reflux for 1 h. To this, Me2SO4 (2.18 mL, 23 mmol) was added dropwise over 10 min. The mixture stirred at reflux for 1 h. The reaction was allowed to cool to room temperature. 10M NaOH was added and the reaction was stirred at room temperature. The mixture was quenched with 10 mL H2O and extracted 3 times with 10 mL dichloromethane. Organic layers were combined and dried over Na2SO4. Solvent was removed under vacuum and the mixture was placed in an 80° C. oil bath under vacuum to remove excess Me2SO4. No further purification was needed to give the product as a black oil (1.31 g, 100% yield). 1H NMR (300 MHz, CDCl3) δ 7.68 (1H, dd, J=8.1, 1.5 Hz), 7.54 (1H, ddd, J=8.7, 7.3, 1.7 Hz), 7.42 (1H, dd, J=7.8, 1.5 Hz), 7.19 (1H, dd, J=7.7, 1.7 Hz), 7.14-7.11 (2H, m), 7.06 (1H, dd, J=7.7, 1.9 Hz), 7.0 (1H, ddd, J=8.2, 7.3, 1.1 Hz); 13C (75 MHz, CDCl3) δ 145.0 (q), 143.0 (q), 133.2 (t), 131.3 (t), 130.9 (q), 128.7 (q), 127.9 (t), 126.7 (t), 126.2 (t), 125.9 (t), 120.8 (t), 120.6 (t), 41.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173803B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-74c2ff7be77e44189688caa260b56002 |
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| Source note | uspto-grants-2012_05 |
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