HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → HCID 70148757, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 1-[1-triphenylmethyl-1H-imidazol-4-yl]-6-cyclohexyl-3-hexyne | HCID 18428375 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70148757 | HCID 70148757 | 101.6% |
Reaction Steps
1-[1-Triphenylmethyl-1H-imidazol-4-yl]-6-cyclohexyl-3-hexyne (6.8 g, 0.014 mol) was dissolved in dry ethyl acetate (100 ml). Lindlar catalyst (5%, 1.8 g Pd on CaCO3 poisoned with lead) and 15 mgs of quinoline were added. H2 was added to the reaction flask via a balloon. The reaction flask was evacuated and then refilled with H2 gas from the balloon 3 times. The reaction was left to stir at room temperature under the presence of H2 (1 atm) for 48 hours. The H2 gas was removed and the reaction mixture filtered through a pad of celite with ethyl acetate, the ethyl acetate was removed in vacuo to afford 6.75 g of 1-[1-triphenylmethyl-1H-imidazol-4-yl]-6-cyclohexyl-cis-3-hexene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448282B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-8a7859bf54184fdabcee492aed2715d3 |
| Source note | uspto-grants-2002_09 |