HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-ethoxalyl-2-ethoxycarbonylethenyltetrahydroquinoline → N-ethoxalyl-2-ethoxycarbonylethyltetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-ethoxalyl-2-ethoxycarbonylethenyltetrahydroquinoline | HCID 67722040 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-ethoxalyl-2-ethoxycarbonylethyltetrahydroquinoline | HCID 67721858 | 95% |
Reaction Steps
N-Ethoxalyl-2-ethoxycarbonylethenyltetrahydroquinoline (4 g, 12.1 mmol) in ethanol (100 mL) was hydrogenated over 10% palladium on carbon (500 mL) under atmospheric pressure of hydrogen for 1.5 h at room temperature. The mixture was filtered through celite and the filtrate was concentrated to give 3.83 g of N-ethoxalyl-2-ethoxycarbonylethyltetrahydroquinoline (95%): 1H NMR (270 MHz, CDCl3) δ7.03~7.19 (m, 4H), 4.78 (m, 1H), 4.11(q, 4H, J 7 Hz), 2.73 (t, 2H, J=6 Hz), 2.47 (m, 1H), 1.69 (m, 1H), 1.25 (t, 3H, J=7 Hz), 1.11 (t, 3H, J=7Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616586 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-7587a164b53b4fe89c612e955bd90768 |
| Source note | uspto-grants-1997_04 |