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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 929459Erstellt: 24. Oktober 2026

Boron trifluoride → (S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-ol

https://huagongshe.com/de/reaction/929459

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluorideHCID 6356—
EduktTrimethylsilylacetyleneHCID 66111—
Edukt(S)-Glycidoxy-t-butyldimethylsilaneHCID 10954307—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-olHCID 86667886—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

tert-Butyl lithium (2 eq) is added to a solution of TMS-acetylene (2 eq) in THF at −78° C. and the reaction mixture stirred for an additional 30 min. (S)-tert-butyldimethyl(oxiran-2-ylmethoxy)silane (1 eq) and BF3.EtO2 (2 eq) are added and stirred at −78° C. for 4.5 hours. The reaction is quenched by addition of aqueous ammonium chloride solution and extracted with ethyl acetate (3×). The combined organic layers are washed with brine, dried (MgSO4) and concentrated under reduced pressure to afford (S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-ol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09296686B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-42a3b186073d4db1b47a7d9f79d75d78
Quellennotizuspto-grants-2016_03