HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 6-Bromo-7-chloro-2-(3,5-dimethylphenyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(3,5-Dimethylphenyl)ethan-1-one | HCID 14921 | — |
| Reactant | (2-Amino-5-bromo-4-chlorophenyl)methanol | HCID 67081018 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Bromo-7-chloro-2-(3,5-dimethylphenyl)quinoline | HCID 86684981 | 43.3% |
Reaction Steps
(2-amino-5-bromo-4-chlorophenyl)methanol (8.2 g, 34.7 mmol), 3,5-dimethylacetophenone (8.22 g, 55.5 mmol), RuCl2(PPh3)3 (0.15 g, 0.173 mmol), and KOH (1.31 g, 23.4 mmol) was refluxed in 90 mL of toluene for 18 hours. Water was collected from the reaction using a Dean-Stark trap. The reaction mixture was allowed to cool to room temperature and filtered through a silica gel plug and eluted with DCM and purified by column chromatography, eluting with 2:1 (v/v) hexanes:DCM, to give 6-bromo-7-chloro-2-(3,5-dimethylphenyl)quinoline (5.2 g, 43.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09217004B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-5b3c372cda554e3b92366ec5f333ff36 |
| Source note | uspto-grants-2015_12 |