Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 502089Erstellt: 25. Oktober 2026

Ammonia → (2-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethynyl)triisopropylsilane

https://huagongshe.com/reaction/502089

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktAmmonium ChlorideHCID 25517—
EduktLithium ChlorideHCID 433294—
Edukt4-Bromo-2-(bromomethyl)-1-chlorobenzeneHCID 11558280—
Edukt((4-Iodophenyl)ethynyl)triisopropylsilaneHCID 57809611—
EduktHCID 178418546HCID 178418546—
EduktHCID 178418918HCID 178418918—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethynyl)triisopropylsilaneHCID 16065644—

Reaktionsbedingungen

Temperatur-25 °C

Reaktionsschritte

Under argon 0.66 ml of a 2 M solution of isopropylmagnesium chloride in tetrahydrofuran are added dropwise to a solution of 0.50 g (4-iodo-phenylethynyl)-triisopropyl-silane in 2.2 ml dry tetrahydrofuran chilled to −25° C. The solution is stirred for 30 min at −25° C. and then combined with 0.26 ml of a 1 M solution of CuCN*2 LiCl in tetrahydrofuran (prepared by dissolving CuCN and LiCl in the ratio 1:2). Shortly afterwards, 0.35 g 4-bromo-2-bromomethyl-1-chlorbenzene are added and the reaction mixture is brought up to −5° C. in the cooling bath. After 6 h stirring at −5° C. the solution is heated to ambient temperature and stirred overnight. Then a mixture of saturated ammonium chloride solution and 25% ammonia solution (9:1) is added and the resulting mixture is added to water. The organic phase is separated off and the aqueous phase is extracted with ethyl acetate, the combined organic phases are dried over sodium sulfate, and the solvent is removed. The residue is purified through silica gel (cyclohexane).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772378B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-721fa65378ed438bac668584e3190458
Quellennotizuspto-grants-2010_08