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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 610785Erstellt: 25. Oktober 2026

Methanol → Methyl 3-hydroxyoctanoate, (S)-

https://huagongshe.com/reaction/610785

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktMethyl 3-oxooctanoateHCID 89668—
EduktHCID 178418361HCID 178418361—
KatalysatorRutheniumHCID 23950—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 3-hydroxyoctanoate, (S)-HCID 1255000295,9%

Reaktionsschritte

Into a 100-ml autoclave (made of Hastelloy) were introduced 20 g of methyl 3-oxooctanoate (manufactured by Inoue Perfumery Mfg. Co., Ltd.) and 50 ml of methanol. The atmosphere in the autoclave was replaced with nitrogen gas. Thereto was added a solution prepared by dissolving 140 mg of Ru2Cl4 ((-)-(T)BINAP)2Et3N as a ruthenium-optically active phosphine complex in 1.0 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 19.4 g of methyl (S)-3-hydroxyoctanoate. Yield, 96%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05998668
Quelldatensatzuspto-grants-1999_12
ORD IDord-4b92dff144d248a589ce7194ce76eebe
Quellennotizuspto-grants-1999_12