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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1646051Erstellt: 27. Oktober 2026

Triethylamine → [(3-Bromophenanthren-9-YL)methoxy](tert-butyl)dimethylsilane

https://huagongshe.com/reaction/1646051

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt4-(Methylamino)pyridineHCID 123098—
Edukt(3-Bromophenanthren-9-YL)methanolHCID 15159129—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[(3-Bromophenanthren-9-YL)methoxy](tert-butyl)dimethylsilaneHCID 1515913087%

Reaktionsschritte

To a solution of 3-bromo-9-(hydroxymethyl) phenanthrene, 4 (5.96 g, 20.8 mmol) and t-butyldimethylsilyl chloride (4.7 g, 31 mmol) in 100 ml of CH2Cl2 and 20 ml of THF was added triethylamine (4.9 ml, 35 mmol) followed by 4-methylaminopyridine (250 mg, 2.05 mmol). After stirring at room temperature for 20 hours, the solution was poured into 300 ml of ethyl ether and washed successively with sat. NH4Cl, sat. NaHCO3, H2O, and brine. Drying (Na2SO4) and evaporation gave a brown solid which was purified by flash chromatography through 400 g of silica gel (1:4 CH2Cl2 -hexane) to yield 7.23 g (87%) of the title compound as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05177202
Quelldatensatzuspto-grants-1993_01
ORD IDord-c0a31e0468614ef7807c6bdae9d610f6
Quellennotizuspto-grants-1993_01