HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(3,5-Dimethylphenyl)-5-(trifluoromethyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(3,5-Dimethylphenyl)ethan-1-one | HCID 14921 | — |
| Reactant | HCID 54486842 | HCID 54486842 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(3,5-Dimethylphenyl)-5-(trifluoromethyl)quinoline | HCID 121266822 | 35.3% |
Reaction Steps
A mixture of (2-amino-6-(trifluoromethyl)phenyl)methanol (18 g, 94 mmol), 1-(3,5-dimethylphenyl)ethanone (19.5 ml, 130 mmol), powdered potassium hydroxide (0.90 g, 16.0 mmol), and RuCl2(PPh3)3 (0.45 g, 0.47 mmol) in toluene (310 ml) was refluxed overnight. Upon cooling to room temperature, the mixture was washed with water and extracted with ethyl acetate (3 times). The crude material was coated on celite and purified by CC starting with 5% EA in Heptanes. The product Obtained was recrystallized from methanol to afford 2-(3,5-dimethylphenyl)-5-(trifluoromethyl)quinoline (10 g, 35% yield) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09397302B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-72f09dc8148e45afacc8d6bc22c4a6e0 |
| Source note | uspto-grants-2016_07 |