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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861533Generated: November 1, 2026

3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl ester → Ethyl 2-ethoxy-3-(4-hydroxyphenyl)propanoate

https://huagongshe.com/reaction/1861533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl esterHCID 11077968—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 1179124397%

Reaction Steps

A mixture of racemic ethyl 2-ethoxy-3-(4-benzyloxyphenyl)propionate of the formula (12a) (40 g) obtained according to the procedure described in step (iv) above, 5% Pd/C catalyst (8 g) and 1,4-dioxane (200 ml) was subjected to hydrogenation at room temperature and 50-60 psi of hydrogen pressure for a period of 8-12 h. The progress of the reaction was monitored by TLC. After completion of the reaction, the catalyst was filtered off and the solvent was removed under reduced pressure,to afford the title compound of the formula (13a) (28-29 g, 97-98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531596B1
Source datasetuspto-grants-2003_03
ORD IDord-a4fe80aeba304bb38e5a46dba6b47c98
Source noteuspto-grants-2003_03