HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389115Generated: October 26, 2026
1-Bromohexadecane → Ethyl 4-hexadecylaminocinnamate
https://huagongshe.com/reaction/1389115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-(4-amino-2-fluorophenyl)prop-2-enoate | HCID 53987187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Ethyl 4-hexadecylaminocinnamate | HCID 53709874 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243609 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-7ace563874104395955cf8557e051695 |
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| Source note | uspto-grants-1981_01 |
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