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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702665Generated: October 31, 2026

1-Bromohexadecane → HCID 54054771, compound

https://huagongshe.com/reaction/1702665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium CarbonateHCID 11430—
ReactantHexamethylphosphoramideHCID 12679—
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
SolventWaterHCID 962—
ProductHCID 54054771HCID 54054771—

Reaction Steps

A solution of 8.2 g. of p-aminophenylacetic acid, 150 ml. of absolute ethanol, and 3 ml. of boron trifluoride etherate is heated to reflux for 15 hrs. The solution is concentrated to ca. 50 ml. by distillation of the solvent 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 p-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 to 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 (4-hexadecylaminophenyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348399
Source datasetuspto-grants-1982_09
ORD IDord-b27e0f66b66e4d9b92b327241ce9a363
Source noteuspto-grants-1982_09