HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl-2,3-epoxy-3-(4-benzyloxyphenyl)propionate → 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl-2,3-epoxy-3-(4-benzyloxyphenyl)propionate | HCID 11277925 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester | HCID 15186153 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223881B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-89f77dd6f67c49f8a7834dbb0eb976a0 |
| Source note | uspto-grants-2007_05 |