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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1825049Erstellt: 24. Oktober 2026

Aluminum isopropoxide → 2-Azido-2-(3-bromophenyl)ethan-1-ol

https://huagongshe.com/de/reaction/1825049

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAluminum isopropoxideHCID 11143—
EduktAzidotrimethylsilaneHCID 78378—
Edukt2-(3-Bromophenyl)oxiraneHCID 147193—
EduktPotassium sodium tartarateHCID 9855836—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Azido-2-(3-bromophenyl)ethan-1-olHCID 2214503129%

Reaktionsschritte

To a solution of 2-(3-bromo-phenyl)-oxirane (2.5 g, 12.6 mmol) in CH2Cl2 (20 mL) was added azidotrimethylsilane (2.5 mL, 18.84 mmol), followed by aluminium isopropoxide (256 mg, 1.26 mmol). The reaction mixture was stirred at room temperature for 18 h. Sodium potassium tartrate 1M (30 mL) was added, the aqueous layer was extracted with CH2Cl2, and the organic layers were dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the crude compound is purified by flash chromatography (10% EtOAc/Hex) to provide 2-azido-2-(3-bromo-phenyl)-ethanol (876 mg, 29%). To a solution of 2-azido-2-(3-bromo-phenyl)-ethanol (876 mg) in THF (10 mL) was added polymer supported triphenylphosphine (3 mmol/g) (2 g, 6 mmol), and the mixture was heated to 60° C. for 30 min. The polymer was then filtered and washed with CH2Cl2. The polymer was suspended in THF (20 mL) and concentrated NH4OH (10 mL) was added, and this mixture was agitated for 24 h. The polymer was filtered and the liquid phase was evaporated in vacuo to afford the title compound (110 mg, 14%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07045551B2
Quelldatensatzuspto-grants-2006_05
ORD IDord-1a34632c1a494f80923ef844923a5cde
Quellennotizuspto-grants-2006_05