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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861561Generated: October 30, 2026

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

https://huagongshe.com/reaction/1861561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl esterHCID 11077968—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 11791243—

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 tetrahydrofuran (120 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 (13 g) (28-29 g, 97-98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531596B1
Source datasetuspto-grants-2003_03
ORD IDord-2b88c7743cd74ecaa7601859e6188a82
Source noteuspto-grants-2003_03