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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11239Erstellt: 25. Oktober 2026

Ethyl trimethylsilylacetate → [1-[5-(4-Fluorobenzyl)furan-2-yl]vinyloxy]-trimethylsilane

https://huagongshe.com/reaction/11239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl trimethylsilylacetateHCID 77687—
Edukt1-[5-[(4-Fluorophenyl)methyl]-2-furanyl]ethanoneHCID 10130640—
KatalysatorTetrabutylammonium FluorideHCID 2724141—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[1-[5-(4-Fluorobenzyl)furan-2-yl]vinyloxy]-trimethylsilaneHCID 2197288388%

Reaktionsschritte

A solution of 2-acetyl-5-(4-fluorobenzyl)furan (10 g, 46 mmol) and trimethylsilylacetic acid ethyl ester (10.9 g, 68 mmol) in anhydrous THF (30 ml) was cooled at −20° C. To a solution was added anhydrous tetrabutylammoniumfluoride (0.2 g). The reaction mixture was gradually warmed up to room temperature and stirred for 15 minutes at 50° C. The THF was evaporated under reduced pressure. The residue was distilled under reduced pressure. The fraction showing b.p. 130° C. (0.5 mmHg) was collected to give [1-[5-(4-fluorobenzyl)furan-2-yl]vinyloxy]-trimethylsilane (11.7 g). Yield 88%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098201B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-719ecd62b0b94a0fbbe448ddbdc6e91c
Quellennotizuspto-grants-2006_08