HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 3-Buten-2-ol, 1,1-dimethoxy-2-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 4,4-Dimethoxy-3-methyl-but-1-yn-3-ol | HCID 12875227 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 3-Buten-2-ol, 1,1-dimethoxy-2-methyl- | HCID 11008050 | — |
Reaction Steps
198 G. of 4,4-dimethoxy-3-methyl-but-1-yn-3-ol are dissolved in 960 ml. of high-boiling petroleum ether and, after the addition of 19.35% palladium catalyst and 19.3 g. of quinoline, hydrogenated under normal conditions. After the uptake of 33.5.1. of hydrogen, the hydrogenation is stopped. The catalyst is filtered off. The filtrate is evaporated under reduced pressure. The remaining 4,4-dimethoxy-3-methyl-but-1-en-3-ol boils, after rectification, at 70°-72° C./18 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061656 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-62fcc790771141dca290e5a598283223 |
| Source note | uspto-grants-1977_12 |