HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 11822048, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl 4-{[(benzyloxy)carbonyl]amino}-3-oxobutanoate | HCID 10265597 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 11822048 | HCID 11822048 | 106.4% |
Reaction Steps
In a 200 ml autoclave were charged 40 g (0.13 mol) of ethyl 4-benzyloxycarbonylamino-3-oxobutyrate, 120 ml of ethanol, and 173 mg (0.102 mmol) of Ru2Cl4((R)-Tol-BINAP)2.NEt3, and asymmetric hydrogenation was carried out at 50° C. under a hydrogen pressure of 30 torr. for 17 hours (conversion: 98.4%; optical purity: 94%e.e.). Ethanol was evaporated under reduced pressure to furnish 38.9 g of the title compound as liquid. An aliquot of the product was purified to find that the yield was 91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403804B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-e4f86c82e5314df6abb9c873c3182e16 |
| Source note | uspto-grants-2002_06 |