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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354913Generated: October 28, 2026

Ethyl-2,3-epoxy-3-(4-benzyloxyphenyl)propionate → 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester

https://huagongshe.com/reaction/1354913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl-2,3-epoxy-3-(4-benzyloxyphenyl)propionateHCID 11277925—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent1,4-DioxaneHCID 31275—
Product3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl esterHCID 1518615380%

Reaction Steps

A mixture of ethyl-2,3-epoxy-3-(4-benzyloxyphenyl)propionate of the formula (9) (125 g) obtained according to the procedure described in step (ii) above, 5% Pd/C catalyst (12.5 g) and 1,4-dioxane (750 ml) was hydrogenated at room temperature at 5–10 psi of hydrogen pressure for a period of 10–15 h The progress of the reaction was monitored by TLC. After completion of the reaction, the catalyst was filtered and the solvent was removed under reduced pressure to afford the title compound of the formula (10) (100–105 g, 80–83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223881B2
Source datasetuspto-grants-2007_05
ORD IDord-89f77dd6f67c49f8a7834dbb0eb976a0
Source noteuspto-grants-2007_05