HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 3-(tetrahydro-2H-pyran-4-yl)-2-propenoate → Ethyl 3-tetrahydro-2H-pyran-4-ylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 3-(tetrahydro-2H-pyran-4-yl)-2-propenoate | HCID 54040092 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-tetrahydro-2H-pyran-4-ylpropanoate | HCID 20143676 | 87.3% |
Reaction Steps
A solution of ethyl 3-(3,4,5,6-tetrahydro-2H-pyran-4-yl)acrylate (17 g) in ethanol (200 ml) is catalytically hydrogenated over 10% palladium-carbon (4 g, 50% wet) at room temperature under atmospheric pressure. After the absorption of hydrogen has ceased, the catalyst is removed by filtration and the filtrate is concentrated in vacuo. The oily residue is purified by vacuum distillation to give ethyl 3-(3,4,5,6-tetrahydro-2H-pyran-4-yl)propionate (15 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04591458 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-9dc1e3945b9d48b8b997ce0ee58592b9 |
| Source note | uspto-grants-1986_05 |