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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483069Erstellt: 24. Oktober 2026

Water → 2-Methoxy-5-nonyl benzophenone

https://huagongshe.com/de/reaction/483069

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktSodium HydroxideHCID 14798—
EduktMethanone, (2-hydroxy-5-nonylphenyl)phenyl-HCID 93939—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Methoxy-5-nonyl benzophenoneHCID 2016199185%

Reaktionsschritte

A sample of 2-hydroxy-5-nonyl benzophenone (25 g, 0.077 mol) was dissolved in 100 mL methylene chloride. To this solution was added a solution of 20 g (0.5 mol) sodium hydroxide in 100 mL deionized water, followed by the addition of 22 g (0.154 mol) iodomethane and 2.5 g (0.006 mol) tetra-n-butylammonium bromide. The entire mixture was agitated with vigorous mechanical stirring for 1.5 hours at 40° C. The reaction mixture was allowed to cool, and the layers separated. The aqueous phase was extracted with 50 mL methylene chloride. The combined organic layers were dried over anhydrous magnesium sulfate and concentrated under vacuum. The residual oil was, taken up in petroleum ether, washed with water, dried over magnesium sulfate and again concentrated under vacuum to provide 22 g (85% yield) of 2-methoxy-5-nonyl benzophenone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04578250
Quelldatensatzuspto-grants-1986_03
ORD IDord-dc8c05e3a8b54dab8a283fe43ae2d743
Quellennotizuspto-grants-1986_03