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HRID 325592Erstellt: 25. Oktober 2026

Triethylamine → 2-(2,6-Dichlorobenzyloxy)ethyl 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate

https://huagongshe.com/reaction/325592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-{4-[4-(Trifluoromethyl)phenoxy]phenoxy}propanoyl chlorideHCID 12906015—
EduktEthanol, 2-((2,6-dichlorophenyl)methoxy)-HCID 13341669—
LösungsmittelTolueneHCID 1140—
Produkt2-(2,6-Dichlorobenzyloxy)ethyl 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionateHCID 1334167093%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

22.1 g of 2-(2,6-dichlorobenzyloxy)ethanol and 10.1 g of triethylamine were dissolved in 200 ml of toluene, then cooled to 0° C. To this solution was dropwise added a solution of 34.5 g of 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionyl chloride in 50 ml of toluene at 0° to 10° C. After the dropwise addition, the reaction mixture was gradually heated and, at 40° C., it was stirred for one hour to complete the reaction. After cooling the reaction solution to room temperature, it was washed successively with 1% strength by weight sodium hydroxide aqueous solution and water, then dehydrated. After distilling off toluene under reduced pressure, the resulting colorless, viscous, oily product was allowed to stand for about 1 month to obtain 49.2 g of crystalline 2-(2,6-dichlorobenzyloxy)ethyl 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate. m.p. 51° to 53° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04441913
Quelldatensatzuspto-grants-1984_04
ORD IDord-81c65e9b7c0842f0b1004984e7e6694b
Quellennotizuspto-grants-1984_04