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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1814335Erstellt: 25. Oktober 2026

Imidazole → (1-Bromo-naphthalen-2-yloxy)-triisopropyl-silane

https://huagongshe.com/reaction/1814335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktPyridineHCID 1049—
Edukt1-Bromo-2-naphtholHCID 11316—
EduktTriisopropylsilyl chlorideHCID 139400—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1-Bromo-naphthalen-2-yloxy)-triisopropyl-silaneHCID 2250424099,1%

Reaktionsschritte

1-Bromo-2-naphthol (5.00 g, 22.4 mmol) was mixed with triisopropylsilyl chloride (7.2 mL, 33.6 mmol), DMAP (402 mg, 3.30 mmol), imidazole (3.81 g, 56.0 mmol), and pyridine (6 mL) in CH2Cl2 (50 mL). The reaction was refluxed for two hours. TLC analysis (silica, 15% EtOAc-hexanes) indicated the reaction was complete. The reaction was allowed to cool to room temperature and then was diluted with H2O. The dilution was extracted three times with CH2Cl2. The organic extracts were combined, washed with brine solution, dried over Na2SO4, filtered through celite, and concentrated. The crude product was purified by flash chromatography (SiO2, 100% hexanes) to give (1-bromo-naphthalen-2-yloxy)-triisopropyl-silane (8.4 g, 22.2 mmol) as a colorless oil in 99% yield. 1H NMR (300 MHz) CDCl3 8.21 (d, J=7.5 Hz, 1H), 7.76 (d, J=8.5 Hz, 1H), 7.68 (d, J=8.8 Hz, 1H), 7.54 (m, 1H), 7.38 (m, 1H), 7.15 (d, J=8.8 Hz, 1H), 1.38 (m, 3H), 1.16 (d, J=7.1 Hz, 18H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06875765B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-cc6ac67d4e814cdcaac13c3e119f2ed4
Quellennotizuspto-grants-2005_04