Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-bromopropyl)-N-methylaniline | HCID 61288549 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71735927 | HCID 71735927 | 24.4% |
Reaction Steps
A mixture of compound 9a (500 mg, 2.7 mmol), K2CO3 (740 mg, 5.4 mmol), and KI (445 mg, 2.7 mmol) in DMF (50 mL) was bubbled with argon for 10 min Hydroquinone (589 mg, 5.4 mmol) was added to the mixture under argon. The reaction mixture was heated and stirred at 80° C. for 6 hours. After cooling to room temperature, the solvent was evaporated and the residue was quenched with 100 mLs water. The mixture was adjusted pH to ˜7 with diluted hydrochloric acid. The mixture was then extracted with CH2Cl2 and the combined organic layer was washed with water and then brine and was dried over Na2SO4. The solvent was evaporated and the residue was purified by silica gel column chromatography with hexane/EtOAc to provide the compound 9 (170 mg, 0.66 mmol, 24% yield) as a white solid. HRMS (ESI, positive) m/z calcd. for C16H20NO2 [M+H]+: 258.14886, found: 258.14888. 1H NMR (400 MHz, Chloroform-d) δ 7.36-7.27 (m, 2H), 6.94-6.70 (m, 7H), 5.94 (broad s, 1H), 4.00 (t, J=5.9 Hz, 2H), 3.60 (t, J=7.0 Hz, 2H), 3.01 (s, 3H), 2.09 (p, J=6.2 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394233B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-3ed6e073011b4103a6d62e36e81689fa |
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| Source note | uspto-grants-2016_07 |
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