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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561420Erstellt: 26. Oktober 2026

Water → (4-Fluoro-2-methylphenyl)(4-fluorophenyl)methanol

https://huagongshe.com/reaction/561420

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-FluorobenzaldehydeHCID 68023—
Edukt2-Bromo-5-fluorotolueneHCID 96743—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(4-Fluoro-2-methylphenyl)(4-fluorophenyl)methanolHCID 58392149—

Reaktionsschritte

1.00 g (5.29 mmol) of 2-bromo-5-fluorotoluene were dissolved in 10 ml of tetrahydrofuran at −78° C. Addition of 4.0 ml (6.35 mmol) of a 1.6N solution of n-butyllithium in hexane was followed by stirring for 15 min, and then 0.79 g (6.35 mmol) of p-fluorobenzaldehyde dissolved in 10 ml of tetrahydrofuran was added dropwise. The mixture was warmed to RT and stirred for 1 h. The reaction solution was mixed with water and ethyl acetate, and the phases were separated. The aqueous phase was extracted three times with ethyl acetate, and the combined organic phases were washed with saturated aqueous sodium chloride solution. The solvents were removed in vacuo, and the crude product was purified by preparative HPLC (mobile phase: acetonitrile-water gradient). 0.56 g (43% of theory) of the title compound was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063234B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-72a9b7629bdb48c7b48f8b0ed345465d
Quellennotizuspto-grants-2011_11