HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 8-Ethyl-2-methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Ethylaniline | HCID 11357 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 8-Ethyl-2-methylquinoline | HCID 14475250 | 59.1% |
Reaction Steps
A solution of 2-ethylaniline (4.00 g, 33.0 mmol) in 6 N HCl (40 mL) was added (E)-but-2-enal (6.20 ml, 75.9 mmol) dropwise at reflux. The reaction was heated at reflux for 3 hours. After cooling to ambient temperature, ethyl acetate (40 mL) was added. The aqueous layer was separated, basified with ammonium hydroxide to about pH 9, and extracted with DCM (2×50 mL). The combined organic layer was dried (sodium sulfate) and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (3:1 hexane/DCM) to give 8-ethyl-2-methylquinoline (3.34 g, 59.1%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889704B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-8396065af8ef454ba60fc6a8f343bfe7 |
| Source note | uspto-grants-2014_11 |