HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633188Generated: October 25, 2026
Triethylamine → beta-Nitrocinnamyl Perfluorooctanoate
https://huagongshe.com/reaction/1633188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Perfluorooctanoyl chloride | HCID 78978 | — |
| Reactant | beta-Nitrocinnamyl alcohol | HCID 54473650 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | beta-Nitrocinnamyl Perfluorooctanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04478967 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-d3e8950b13bb47d088070983be7843b2 |
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| Source note | uspto-grants-1984_10 |
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