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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156137Generated: October 25, 2026

1-Bromohexadecane → Ethyl 2-fluoro-4-(hexadecylamino)phenylacetate

https://huagongshe.com/reaction/1156137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium CarbonateHCID 11430—
ReactantHexamethylphosphoramideHCID 12679—
ReactantEthyl 2-(4-amino-2-fluorophenyl)acetateHCID 15840528—
SolventWaterHCID 962—
ProductEthyl 2-fluoro-4-(hexadecylamino)phenylacetateHCID 54400635—

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-60af6d9b24e94573894a371e7b90a29a
Source noteuspto-grants-1982_06