HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxy-2-methylquinoline → 5,6,7,8-Tetrahydro-3-methoxy-2-methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxy-2-methylquinoline | HCID 12820971 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5,6,7,8-Tetrahydro-3-methoxy-2-methylquinoline | HCID 22036993 | 99.6% |
Reaction Steps
A mixture of 3-methoxy-2-methylquinoline (0.081 mol) in trifluoro-acetic acid (150 ml) was hydrogenated at room temperature under a 34 bar pressure for 48 hours with palladium on activated carbon (2 g) as a catalyst. After uptake of hydrogen (2 equiv.), the catalyst was filtered through celite and washed with H2O. The filtrate was basified with a concentrated NH4 OH solution and extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated, yielding 14.3 g (quant.) of 5,6,7,8-tetrahydro-3-methoxy-2-methylquinoline (interm. 13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071192B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-e14ca53373f947628d9a61d018702f84 |
| Source note | uspto-grants-2006_07 |