HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 2,4-Diisopropylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 3,5-Diisopropylsalicylic acid | HCID 30543 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,4-Diisopropylphenol | HCID 18048 | 102% |
Reaction Steps
A mixture of 3,5-diisopropylsalicylic acid (Intermediate 9, 25 g, 0.11 mol, available from Aldrich) and quinoline (50 mL) was refluxed for 4 h. The mixture was cooled to room temperature, diluted with EtOAc (200 mL), washed with 1M HCl (2×200 mL) until acidic, then with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (5% then 10% EtOAc-hexanes) to yield the title compound as a yellow oil (20 g, ˜100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06759546B1 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-c0ee3cf0b56346188347ffa2d8b796d3 |
| Source note | uspto-grants-2004_07 |