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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 502086Erstellt: 27. Oktober 2026

Water → (5-Bromo-2-fluoro-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}methanol

https://huagongshe.com/reaction/502086

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt5-Bromo-2-fluorobenzaldehydeHCID 736327—
Edukt((4-Bromophenyl)ethynyl)triisopropylsilaneHCID 57809595—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt(5-Bromo-2-fluoro-phenyl)-{4-[(triisopropylsilyl)-ethynyl]-phenyl}methanolHCID 57809581—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

33.8 ml of a 1.6 M solution of n-butyllithium in hexane are added dropwise under argon to a solution of 17.4 g 1-bromo-4-triisopropylsilylethynyl-benzene in 120 ml dry tetrahydrofuran chilled to −78° C. The solution is stirred for 1 h at −70° C. Then 10.8 g 5-bromo-2-fluoro-benzaldehyde dissolved in 30 ml of tetrahydrofuran are added dropwise over 15 min. The resulting solution is left in the cooling bath to warm up overnight to ambient temperature. Then water is added and the mixture is extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate, and the solvent is removed. The residue is purified by chromatography on silica gel (cyclohexane/ethyl acetate 4:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772378B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-3b97036ce2fc459983c368fedd82de3e
Quellennotizuspto-grants-2010_08