HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinoline → 2-[6-[(6-Bromohexyl)oxy]hexyl]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinoline | HCID 19876759 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[6-[(6-Bromohexyl)oxy]hexyl]quinoline | HCID 22161737 | 73.5% |
Reaction Steps
A solution of 2-[6-[(6-bromohexyl)oxy]-1-hexynyl]quinoline (2.29 g) in ethanol (120 ml) was hydrogenated at room temperature and pressure over pre-reduced 10% palladium on carbon (1 g) for 20 min. The catalyst was removed by filtration through hyflo and the filtrate evaporated in vacuo to a brown oil. Purification by FCC eluting with hexane-ether (2:1) gave the title compound as a pale brown oil (1.70 g), t.l.c. (hexane:ether 2:1) Rf 0.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963564 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-76eac424e8314a9f9f41d04ae64f749b |
| Source note | uspto-grants-1990_10 |