HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112379Generated: November 3, 2026
Phosphate → Ethyl 2-hydroxy-4-phenylbutyrate, (+-)-
https://huagongshe.com/reaction/2112379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | Ethyl alpha-oxobenzenebutanoate | HCID 562087 | — |
| Catalyst | Nadide (JAN/USAN/INN) | HCID 5893 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | Ethyl 2-hydroxy-4-phenylbutyrate, (+-)- | HCID 4092621 | 99% |
Reaction Steps
3.0 g of ethyl 2-oxo-4-phenylbutyrate, 0.49 g of the above-mentioned wet cell, 3.0 mg of NAD+, 4.5 g of glucose, 30 ml of 100 mM phosphate buffering solution (pH 7.0) and 6 ml of butyl acetate were mixed and stirred at 30° C. for 9 hours. During stirring, 2M sodium carbonate aqueous solution was added gradually so that the reaction solution had a pH of 7.0. Thereafter, to the reaction liquid was added 50 ml of ethyl acetate, then, centrifugal separation was performed to obtain an organic layer. This organic layer was dehydrated over magnesium sulfate, and ethyl acetate was distilled off, to obtain 3.0 g of ethyl 2-hydroxy-4-phenylbutyrate. The optical purity of the resulting ethyl 2-hydroxy-4-phenylbutyrate was measured, to find 100% e.e. for (R) configuration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07524666B2 |
|---|
| Source dataset | uspto-grants-2009_04 |
|---|
| ORD ID | ord-34aaaf1a07634eae99328441b588f06e |
|---|
| Source note | uspto-grants-2009_04 |
|---|