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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1591358Erstellt: 27. Oktober 2026

Methyl 2-((benzoylamino)methyl)-3-oxobutanoate → Methyl 2-(benzamidomethyl)-3-hydroxybutanoate

https://huagongshe.com/reaction/1591358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 2-((benzoylamino)methyl)-3-oxobutanoateHCID 11831808—
EduktHCID 178418361HCID 178418361—
LösungsmittelDichloromethane methanolHCID 21226129—
ProduktMethyl 2-(benzamidomethyl)-3-hydroxybutanoateHCID 1976684378%

Reaktionsschritte

Into a 200-ml stainless steel-made autoclave was placed 3.56 g (0.0143 mole) of methyl 2-benzamidomethyl-3-oxobutyrate. After nitrogen replacement, 7 ml of a separately prepared dichloromethane/methanol (7/1 by volume) mixed solvent solution containing 0.01 g (0.00894 mmole) of [RuI(p-Cymene)((-)-OcH-BINAP)]I as obtained in Example 5 was added. The resulting mixture was stirred at a hydrogen pressure of 50 kg/cm2 and a temperature of 65° C. for 20 hours. After the reaction, the reaction mixture was analyzed- by high-speed liquid chromatography. As a result, it was found that 2.79 g (percent yield: 78%) of methyl 2-benzamidomethyl-3-hydroxybutyrate had been formed and that the conversion was 80%, diastereomer selectivity 91.6%, and optical percent yield 99% ee.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05206399
Quelldatensatzuspto-grants-1993_04
ORD IDord-9f6649b1cbc34032a1d7575ebb5261f7
Quellennotizuspto-grants-1993_04