Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655725Erstellt: 25. Oktober 2026

Magnesium trifluoromethanesulfonate → (R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoate

https://huagongshe.com/reaction/655725

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMagnesium trifluoromethanesulfonateHCID 2734125—
EduktMethyl (2R)-2-oxiranecarboxylateHCID 9877347—
Edukt(S)-1-(triisopropylsilyloxy)propan-2-olHCID 57504699—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoateHCID 8664084741,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Magnesium trifluoromethanesulfonate (1.263 g, 3.92 mmol) was added to a mixture of (S)-1-(triisopropylsilyloxy)propan-2-ol (4.55 g, 19.59 mmol) and (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) in ethyl acetate (40 mL). The resulting suspension was heated to 80° C. for 72 hours. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred at 80° C. for 48 hrs. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred for 24 hrs. The mixture was allowed to cool, filtered through a bed of silica (˜10 g), washed through with EtOAc and evaporated. The crude product was purified by flash silica chromatography, elution gradient 10 to 50% EtOAc in isohexane, to afford the product (2.7 g, 41%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071608B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-786616f159c04a1491d48599f08480bf
Quellennotizuspto-grants-2011_12