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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389115Generated: October 26, 2026

1-Bromohexadecane → Ethyl 4-hexadecylaminocinnamate

https://huagongshe.com/reaction/1389115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-(4-amino-2-fluorophenyl)prop-2-enoateHCID 53987187—
SolventWaterHCID 962—
SolventHexamethylphosphoramideHCID 12679—
ProductEthyl 4-hexadecylaminocinnamateHCID 53709874—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 2-fluoro-4-aminocinnamate, one equivalent of 1-bromohexadecane and one equivalent of anhydrous potassium carbonate in hexamethylphosphoramide is heated for 20 hours at 60° C. The mixture is then cooled, diluted with water and extracted with ether. The combined ether extracts are dried, filtered and evaporated to provide ethyl 4-hexadecylaminocinnamate. The ester is hydrolyzed with sodium hydroxide in a 1:9 water:ethanol solution at steam bath temperatures for 10 hours. The hot solution is then acidified with acetic acid, cooled and filtered and the solid is washed with water. Recrystallization from chloroform yields 2-fluoro-4-(hexadecylamino)cinnamic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243609
Source datasetuspto-grants-1981_01
ORD IDord-7ace563874104395955cf8557e051695
Source noteuspto-grants-1981_01