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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Boron trifluoride | HCID 6356 | — |
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | (S)-Glycidoxy-t-butyldimethylsilane | HCID 10954307 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-ol | HCID 86667886 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09296686B2 |
|---|
| Quelldatensatz | uspto-grants-2016_03 |
|---|
| ORD ID | ord-42a3b186073d4db1b47a7d9f79d75d78 |
|---|
| Quellennotiz | uspto-grants-2016_03 |
|---|