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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458125Erstellt: 25. Oktober 2026

Dimethyl Sulfide → 4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-one

https://huagongshe.com/reaction/458125

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfideHCID 1068—
EduktChlorotrimethylsilaneHCID 6397—
EduktMesityl oxideHCID 8858—
Edukt2-Bromo-4-fluoroanisoleHCID 136292—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 2228492285%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a stirred solution of 2-bromo-4-fluoro anisole (3.24 mL, 25 mmol) in anhydrous THF (40 mL) cooled to −78° C. and maintained under argon was added n-butyl lithium (17.2 mL of 1.6 M solution in hexanes, 27.5 mmol). After stirring at −78° C. for 45 minutes, the reaction mixture was treated with a solution of cuprous iodide in dimethyl sulfide (4.76 g in 15 mL, 25 mmol) and stirred for 15 minutes at −78° C. Then chlorotrimethylsilane (6.4 mL, 50 mmol) was added, followed by a solution of mesityl oxide (2.9 mL, 25 mmol) in anhydrous THF (5 mL). The reaction was stirred at −78° C. to −60° C. for 4 hours and then quenched with a saturated solution of ammonium chloride and extracted with three 50 mL portions of methylene chloride. The combined extracts were washed with three 25 mL portions of water, dried over anhydrous sodium sulfate, and concentrated in vacuo to give 4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-one as a light brown liquid (85% yield) which was used in the next reaction without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189758B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-c8ea7327285d4c5887ed3c45b93c981d
Quellennotizuspto-grants-2007_03