HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178516272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 18511451 | HCID 18511451 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178516272 | HCID 178516272 | 73% |
Reaction Steps
A solution of 2-bromo-α-cyclohexyl-4-quinolinemethanol (100 mg, 0.31 mmol) in dioxan (1 mL) was treated with 1-M HCl, stirred at room temperature for 16 h, refluxed for 24 h, cooled, diluted with water (5 mL), the resulting solid filtered and dried under vacuum to give the title compound (58 mg, 73%) as a white solid: mp>250° C.; IR νmax (Nujol)/cm−1 3451, 2956, 2924, 2854, 1649, 1546, 1437, 1103, 886 and 760; NMR δH (400 MHz, DMSO-d6) 1.07-1.29 (5H, m), 1.53-1.69 (6H, m), 4.77 (1H, t, J 4.5 Hz), 5.38 (1H, d, J 4.6 Hz), 6.50 (1H, s), 7.18 (1H, t, J 7.0 Hz), 7.34 (1H, d, J 7.6 Hz), 7.49 (1H, t, J 7.0 Hz), 7.84 (1H, d, J 7.6 Hz) and 11.64 (1H, s); M/Z 258 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583156B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-624f224ca0054bfd865ae3e1c22b7cc6 |
| Source note | uspto-grants-2003_06 |