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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49344Erstellt: 24. Oktober 2026

Triethylamine → [(e)-5-(4-Bromo-2-thienyl)-1,1-diethylhept-4-enyloxy]triethylsilane

https://huagongshe.com/de/reaction/49344

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-DimethylaminopyridineHCID 21885—
EduktTriethylsilyl trifluoromethanesulphonateHCID 2733308—
Edukt(e)-7-(4-Bromo-2-thienyl)-3-ethylnon-6-en-3-olHCID 69824523—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt[(e)-5-(4-Bromo-2-thienyl)-1,1-diethylhept-4-enyloxy]triethylsilaneHCID 69825241—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

11.8 g (35.6 mmol) of (E)-7-(4-bromo-2-thienyl)-3-ethylnon-6-en-3-ol are dissolved in 150 mL of dichloromethane. 130 mg (1.1 mmol) of dimethylaminopyridine and 14.9 mL (107 mmol) of triethylamine are added. The reaction medium is cooled to 0° C. and 12.1 mL (53.4 mmol) of triethylsilyl trifluoromethanesulphonate are added dropwise. The medium is warmed to room temperature and stirred for 15 minutes, after which it is poured into 150 mL of water and extracted with dichloromethane. After chromatography on silica gel (eluent: heptane), the desired product is obtained in the form of a colourless oil (m=15 g; Y=100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706725B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-61c3221b133044d69ab1c621e42a83c4
Quellennotizuspto-grants-2004_03