HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 1,6-Dicarbomethoxy-cis-3-hexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 1,6-Dicarbomethoxy-3-hexyne | HCID 10954517 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,6-Dicarbomethoxy-cis-3-hexene | HCID 23272983 | 93.1% |
Reaction Steps
A mixture of 1,6-dicarbomethoxy-3-hexyne [II-1] (5 g), a Lindlar catalyst (5% Pd-CaCO3 -PbO) (50 mg), quinoline (25 mg) and methanol (15 ml) is charged in an atmospheric hydrogenation apparatus and subjected to reduction at room temperature under atmospheric pressure. After completion of the reaction, the catalyst is removed by filtration and the filtrate is concentrated to give 1,6-dicarbomethoxy-cis-3-hexene [II-2] (4.70 g, yield; 93.0%), b.p. 92°-95° C./0.3 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05191109 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-cd04e879614c41f980684f008036c460 |
| Source note | uspto-grants-1993_03 |