HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (-)-Methyl (R)-3-hydroxyvalerate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl 3-oxovalerate | HCID 121699 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (-)-Methyl (R)-3-hydroxyvalerate | HCID 11804797 | 98.1% |
Reaction Steps
Into a 200-ml autoclave (made of Hastelloy) were introduced 50 g of methyl 3-oxopentanoate (manufactured by Wacker Chemicals Co., Ltd.) and 75 ml of methanol. The atmosphere in the autoclave was replaced with nitrogen gas. Thereto was added a solution prepared by dissolving 325 mg of Ru2Cl4 ((+)-(T)BINAP)2Et3N as a ruthenium-optically active phosphine complex in 3.8 ml of methylene chloride. Asymmetric hydrogenation was conducted at a reaction temperature of 30° C. and a hydrogen pressure of 30 atm. After the reaction mixture was thus reacted for 50 hours, it was taken out of the autoclave. The methanol was distilled off, and the residue was subjected to vacuum distillation to obtain 49.8 g of methyl (R)-3-hydroxypentanoate. Yield, 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998668 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-5dd474b8bae8449a987aa14641c66661 |
| Source note | uspto-grants-1999_12 |