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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354888Generated: October 25, 2026

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

https://huagongshe.com/reaction/1354888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Benzyloxyphenyl)-2-ethoxypropanoic acid ethyl esterHCID 11077968—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-OxathianeHCID 27596—
ProductEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 1179124397%

Reaction Steps

A mixture of racemic ethyl 2oxy-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-thioxane (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 numberUS07223881B2
Source datasetuspto-grants-2007_05
ORD IDord-b8e5f116950147cf9a865c6a834c27c4
Source noteuspto-grants-2007_05