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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1814336Erstellt: 25. Oktober 2026

Ethylene Oxide → 2-(2-Triisopropylsilanyloxy-naphthalen-1-yl)-ethanol

https://huagongshe.com/reaction/1814336

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene OxideHCID 6354—
EduktBoron trifluoride etherateHCID 8000—
Edukt(1-Bromo-naphthalen-2-yloxy)-triisopropyl-silaneHCID 22504240—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(2-Triisopropylsilanyloxy-naphthalen-1-yl)-ethanolHCID 2250401553%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

n-Butyllithium (16.4 mL of 1.6 M soln in hexanes, 26.3 mmol) was stirred with Et2O (60 mL) at −78° C. in an argon-purged, round-bottom flask. A solution of (1-bromo-naphthalen-2-yloxy)-triisopropyl-silane (7.10 g, 18.8 mmol) in Et2O (˜5 ml) was added dropwise to the stirring n-BuLi solution. The reaction was stirred at −78° C. for ten minutes and then a solution of ethylene oxide (1.41 mL, 28.2 mmol) and BF3-Et2O (3.81 mL, 31.0 mmol) in Et2O (˜5 ml) was added via syringe. The reaction was stirred at −78° C. for one hour and then at room temperature for two hours. The reaction was carefully quenched with H2O and was extracted three times with EtOAc. The organic extracts were combined, washed with brine solution, dried over Na2SO4, filtered through celite, and concentrated. The crude product was purified by gradient elution flash chromatography (SiO2, 100% hexanes to 10% EtOAc-hexanes) to give 2-(2-triisopropylsilanyloxy-naphthalen-1-yl)-ethanol (3.41 g, 9.91 mmol) as a colorless oil in 53% yield. MS (APCI) m/z 343.2 (M−1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06875765B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-8eb0ad6b3ca048bf9b5a1318cc9004c8
Quellennotizuspto-grants-2005_04