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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354884Generated: November 1, 2026

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

https://huagongshe.com/reaction/1354884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl-2,3-epoxy-3-(4-benzyloxyphenyl)propionateHCID 11277925—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
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, Raney Nickel catalyst (12.5 g) and 1,4-dioxane (750 ml) was hydrogenated at room temperature at 30–40 psi of hydrogen pressure for a period of 8–10 hours. 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-793449a2511841c5b16438a42a622d95
Source noteuspto-grants-2007_05