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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 862069Erstellt: 24. Oktober 2026

Water → (4-Methoxymethoxy-phenylethynyl)-trimethylsilane

https://huagongshe.com/de/reaction/862069

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktChlorotrimethylsilaneHCID 6397—
Edukt4-(2,2-Dibromoethenyl)phenol methoxymethyl etherHCID 54096825—
EduktHCID 178418244HCID 178418244—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4-Methoxymethoxy-phenylethynyl)-trimethylsilaneHCID 10657368—

Reaktionsschritte

A solution of 4-(2,2-dibromoethenyl)phenol methoxymethyl ether (16.56 g) in THF (350 ml) was cooled to -78° C., to which was added dropwise, under argon atmosphere, a 1.6M n-butyl lithium hexane solution (70 ml). The mixture was stirred for one hour under the same conditions, which was then warmed and stirred for one hour at room temperature. The reaction mixture was cooled with ice, to which was added dropwise trimethylchlorosilane (7.2 ml). The mixture was then stirred for 3 hours while warming up to room temperature, to which was added water to quench the reaction, followed by extraction with ethyl acetate. The organic layer was washed (a saturated aqueous saline solution) and dried (anhydrous magnesium sulfate), then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 4-(2-trimethylsilylethynyl)phenol methoxymethyl ether (10.76 g) (Compound B-26). The physical properties are shown in Table 8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05716971
Quelldatensatzuspto-grants-1998_02
ORD IDord-6b044bd90cf64d54978473a34cffc4cc
Quellennotizuspto-grants-1998_02