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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Ethyl 2-(4-amino-2-fluorophenyl)acetate | HCID 15840528 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-fluoro-4-(hexadecylamino)phenylacetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04333940 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-60af6d9b24e94573894a371e7b90a29a |
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| Source note | uspto-grants-1982_06 |
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