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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280987Generated: October 29, 2026

ethyl 3-(tetrahydro-2H-pyran-4-yl)-2-propenoate → Ethyl 3-tetrahydro-2H-pyran-4-ylpropanoate

https://huagongshe.com/reaction/280987

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 3-(tetrahydro-2H-pyran-4-yl)-2-propenoateHCID 54040092—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductEthyl 3-tetrahydro-2H-pyran-4-ylpropanoateHCID 2014367687.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591458
Source datasetuspto-grants-1986_05
ORD IDord-9dc1e3945b9d48b8b997ce0ee58592b9
Source noteuspto-grants-1986_05