HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-(benzyloxy)-3-oxobutanoate → ethyl(S)-4-benzyloxy-3-hydroxybutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-(benzyloxy)-3-oxobutanoate | HCID 9813448 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl(S)-4-benzyloxy-3-hydroxybutyrate | HCID 8030429 | 87% |
Reaction Steps
300.0 g (1.27 moles) ethyl 4-benzyloxy-3-oxobutyrate, 300 ml ethanol, and 104.5 mg (0.127 mmol) [RuCl{(R)-segphos}]2(μ-Cl)3 [Me2NH2] were introduced in a nitrogen stream into a 1-L autoclave and flushed with hydrogen, and after introduction of hydrogen at a pressure of 1 MPa, the mixture was heated with stirring. The mixture was reacted at 90 to 95° C. for 7 hours. After the reaction solution was cooled to room temperature, the hydrogen was purged and replaced by nitrogen. The reaction solution was concentrated in a rotary evaporator and the residue was distilled under reduced pressure to give 263.3 g of the title compound (chemical purity, 96.2%; optical purity, 99.1% ee; and yield, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608214B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-6653db0ca57245e3b5cfcead20d36c84 |
| Source note | uspto-grants-2003_08 |