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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458121Erstellt: 24. Oktober 2026

Acetone → 2-(5-Fluoro-2-methoxyphenyl)propan-2-ol

https://huagongshe.com/de/reaction/458121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
Edukt2-Bromo-4-fluoroanisoleHCID 136292—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(5-Fluoro-2-methoxyphenyl)propan-2-olHCID 2228488885%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a stirred solution of 2-bromo-4-fluoro anisole (4.1 g, 20 mmol) in anhydrous THF (40 mL) cooled to −78° C. and maintained under an atmosphere of argon was added n-butyl lithium (8.8 mL of 2.5 M solution in hexanes, 22 mmol). After stirring at −78° C. for 45 minutes, the reaction mixture was treated with anhydrous acetone (5 mL). After 15 minutes, the reaction mixture was quenched with a saturated solution of ammonium chloride and extracted with three 50 mL portions of methylene chloride. Combined extracts were washed with three 25 mL portions of water, dried over anhydrous sodium sulfate, and the solvent was evaporated to give 2-(5-fluoro-2-methoxyphenyl)propan-2-ol as a light brown thick oil (85% yield) which solidified on standing. The crude product was used for the next reaction without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189758B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-f5210dcb51a346028c940970d24e133b
Quellennotizuspto-grants-2007_03