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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389110Generated: October 26, 2026

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

https://huagongshe.com/reaction/1389110

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 numberUS04243609
Source datasetuspto-grants-1981_01
ORD IDord-fa39b9bf62614413b0126e5f379c86ab
Source noteuspto-grants-1981_01