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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633188Generated: October 25, 2026

Triethylamine → beta-Nitrocinnamyl Perfluorooctanoate

https://huagongshe.com/reaction/1633188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPerfluorooctanoyl chlorideHCID 78978—
Reactantbeta-Nitrocinnamyl alcoholHCID 54473650—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Productbeta-Nitrocinnamyl PerfluorooctanoateHCID 53639101—

Reaction Steps

β-Nitrocinnamyl alcohol (5.4 g, 0.03 mol) and one equivalent of triethylamine (3.03 g, 0.03 mol) were dissolved in 100 M of toluene. The solution was cooled in an ice bath and perfluorooctanoyl chloride (2.6 g, 0.03 mol) was added dropwise with stirring. The reaction was stirred an addtional two hours and diluted with ether. The reaction was extracted with water and the organic layer was dried over anhydrous magnesium sulfate and evaporated in vacuo. The oily product was crystallized from petroleum ether to give yellow prisms, mp 79-81°, IR 1785, 1655, 1535, 1325, and 1200 cm-1. A solution of the material in 95% ethanol showed an absorption of λmax at 302 nm, epsilon=10,800 which rapidly decreased on exposure to the GE H3T7 source. This loss of the 302 nm absorption was accompanied by a decrease in the pH (increased acidity) of the solution as as indicated by methyl red pH indicator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04478967
Source datasetuspto-grants-1984_10
ORD IDord-d3e8950b13bb47d088070983be7843b2
Source noteuspto-grants-1984_10