HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610784Generated: October 25, 2026
Methanol → Methyl (3R)-3-hydroxyoctanoate
https://huagongshe.com/reaction/610784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl 3-oxooctanoate | HCID 89668 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl (3R)-3-hydroxyoctanoate | HCID 12550001 | 94.9% |
Reaction Steps
Into a 100-ml autoclave (made of Hastelloy) were introduced 20 g of methyl 3-oxooctanoate (manufactured by Inoue Perfumery Mfg. Co., Ltd., Japan) and 40 ml of methanol. The atmosphere in the autoclave was replaced with nitrogen gas. Thereto was added a solution prepared by dissolving 150 mg of Ru2Cl4 ((+)-(T)BINAP)2Et3N as a ruthenium-optically active phosphine complex in 1.2 ml of methylene chloride. Asymmetric hydrogenation was conducted at a reaction temperature of 65° C. and a hydrogen pressure of 30 atm. After the reaction mixture was thus reacted for 6 hours, it was taken out of the autoclave. The methanol was distilled off, and the residue was subjected to vacuum distillation to obtain 19.2 g of methyl (R)-3-hydroxyoctanoate. Yield, 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998668 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-b2e67f5beaa14cc2bd688aa78a597b6a |
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| Source note | uspto-grants-1999_12 |
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