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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156136Generated: October 25, 2026

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

https://huagongshe.com/reaction/1156136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-(4-Amino-2-fluorophenyl)acetic acidHCID 18794349—
SolventEthanolHCID 702—
ProductEthyl 2-(4-amino-2-fluorophenyl)acetateHCID 15840528—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04333940
Source datasetuspto-grants-1982_06
ORD IDord-d78aa7fd01754074bc40784b50efe0be
Source noteuspto-grants-1982_06