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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2263588Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2263588

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 phase are dried over sodium sulphate, and the solvent is removed. The residue is purified through silica gel (cyclohexane/ethyl acetate 4:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07851602B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-8054f41ef21e44f896bb7df00f31e0b4
Quellennotizuspto-grants-2010_12