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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29918Erstellt: 23. Oktober 2026

Benzoyl chloride → 2-Benzoyl-5-methoxybenzoic acid

https://huagongshe.com/de/reaction/29918

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktHexaneHCID 8058—
Edukt2-Bromo-5-methoxybenzoic acidHCID 89906—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Benzoyl-5-methoxybenzoic acidHCID 334080—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of 2-bromo-5-methoxybenzoic acid (5 g, 21.6 mmol) in 50 mL of THF is stirred under argon at −78° C., and a 1.6 M solution of n-butyllithium in hexane (29 mL, 45 mmol) is then added dropwise. The reaction mixture is stirred for 1 hour at −78° C. and benzoyl chloride (3.2 g, 22.7 mmol) is then added dropwise. The reaction mixture is stirred for 1 hour 30 minutes at −78° C. and then for 18 hours at room temperature. The mixture is hydrolysed with 100 mL water and then washed with ethyl acetate. The aqueous phase is acidified by addition of 5 N hydrochloric acid and then extracted with ethyl acetate. The organic phase obtained is washed with brine and then dried over anhydrous sodium sulfate. After filtration and evaporation under reduced pressure, 5.4 g of a colourless oil are obtained, and are used without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423030B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-925758cac70f47c8b4ab12e182b17ff3
Quellennotizuspto-grants-2008_09