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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325594Erstellt: 26. Oktober 2026

1-Chloro-4-(trifluoromethyl)benzene → 2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate

https://huagongshe.com/reaction/325594

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
EduktPotassium CarbonateHCID 11430—
Edukt2-(2-Fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionateHCID 13278922—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionateHCID 13132188—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

33.4 g of 2-(2-fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionate was dissolved in 120 ml of dimethylformamide, 15.2 g of potassium carbonate were added thereto, then the mixture was heated at 95° C. for one hour with stirring. 27.1 g of 4-trifluoromethyl chlorobenzene were added to the solution which was then heated to 95° to 100° C. for five hours. After cooling the reaction solution to room temperature, it was poured into ice-water, then extracted with toluene. The toluene layer was washed successively with 1% strength by weight sodium hydroxide solution and water, and was dried and filtered. The toluene was distilled off under reduced pressure, and further volatile by-products were removed at 100° C./0.1 mmHg. The end product of 2-(2-fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate was obtained in a yield of 20.7 g. (nD20 1.5235)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04441913
Quelldatensatzuspto-grants-1984_04
ORD IDord-917c4f4b5fc74a62becab5a37151707f
Quellennotizuspto-grants-1984_04