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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl 2-((benzoylamino)methyl)-3-oxobutanoate | HCID 11831808 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dichloromethane methanol | HCID 21226129 | — |
| Produkt | Methyl 2-(benzamidomethyl)-3-hydroxybutanoate | HCID 19766843 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05206399 |
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| Quelldatensatz | uspto-grants-1993_04 |
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| ORD ID | ord-9f6649b1cbc34032a1d7575ebb5261f7 |
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| Quellennotiz | uspto-grants-1993_04 |
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