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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1583583Erstellt: 25. Oktober 2026

Dimethylformamide → Ethyl 3-(2-fluoroethoxy)benzoate

https://huagongshe.com/reaction/1583583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt1-Chloro-2-fluoroethaneHCID 12983—
EduktEthyl 3-hydroxybenzoateHCID 24522—
LösungsmittelWaterHCID 962—
ProduktEthyl 3-(2-fluoroethoxy)benzoateHCID 1505863385,1%

Reaktionsschritte

Thirty grams of ethyl 3-hydroxybenzoate, 14.9 g of 1-fluoro-2-chloroethane and 37.4 g of anhydrous potassium carbonate were added to 130 ml of dimethylformamide. With stirring, the reaction was carried out at 120° C. for 4 hours. The reaction mixture was cooled to room temperature, poured into water, and extracted with toluene. The toluene layer was washed with water, and dried over anhydrous sodium sulfate. Toluene was evaporated under reduced pressure to give 32.6 g of crude ethyl 3-(2-fluoroethoxy)benzoate. The resulting crude ethyl 3-(2-fluoroethoxy)benzoate (32.6 g) was added at 40° to 45° C. to a solution of 6.0 g of lithium aluminum hydride in 200 ml of dry tetrahydrofuran, and the mixture was heated under reflux for 2 hours. After the reaction, the reaction mixture was cooled to room temperature. Ethanol and water in this order were added to the mixture to decompose the unreacted lithium aluminum hydride. Water was then added, and the mixture was extracted with toluene. The toluene layer was washed with water, and dried over anhydrous sodium sulfate. Toluene was removed to give 26.0 g of crude 3-(2-fluoroethoxy)benzyl alcohol This compound was chlorinated to give 30.0 g of 3-(2-fluoroethoxy)benzyl chloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04552894
Quelldatensatzuspto-grants-1985_11
ORD IDord-3f744ca3762f42798fc66784e4344780
Quellennotizuspto-grants-1985_11