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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156142Generated: October 26, 2026

1-Bromohexadecane → Ethyl 4-hexadecylaminocinnamate

https://huagongshe.com/reaction/1156142

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 numberUS04333940
Source datasetuspto-grants-1982_06
ORD IDord-03c5fbe2059e4c70b4006d3fb7efee4f
Source noteuspto-grants-1982_06