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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1389109Erstellt: 26. Oktober 2026

Boron trifluoride etherate → Ethyl 2-(4-amino-2-fluorophenyl)acetate

https://huagongshe.com/reaction/1389109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
Edukt2-(4-Amino-2-fluorophenyl)acetic acidHCID 18794349—
LösungsmittelEthanolHCID 702—
ProduktEthyl 2-(4-amino-2-fluorophenyl)acetateHCID 15840528—

Reaktionsschritte

A solution of 8.2 g. of 2-fluoro-4-aminophenylacetic acid, 150 ml. of absolute ethanol, and 3 ml. of boron trifluoride etherate is heated to reflux for 15 hours. The solution is concentrated by distillation and then evaporated to dryness in vacuo. The residue is dissolved in ethyl ether, washed with aqueous sodium bicarbonate dried and evaporated to yield ethyl 2-fluoro-4-aminophenylacetate. A mixture of 5.0 g. of this amine, 9.4 g. of 1-bromohexadecane, 4.2 g. of anhydrous potassium carbonate and 40 ml. of hexamethylphosphoramide is heated at 80° C. for 7 hours. The mixture is then cooled, diluted with water, and extracted with ethyl ether. The ether extracts are washed with water, dried and evaporated. The residue is recrystallized from a mixture of chloroform and hexane, yielding ethyl 2-fluoro-4-(hexadecylamino)phenylacetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04243609
Quelldatensatzuspto-grants-1981_01
ORD IDord-2230d1c91d4b4619a4d42646b17d8c06
Quellennotizuspto-grants-1981_01