![27905-45-9](/CAS/GIF/27905-45-9.gif)
1H,1H,2H,2H-Heptadecafluorodecyl acrylate synthesis
- Product Name:1H,1H,2H,2H-Heptadecafluorodecyl acrylate
- CAS Number:27905-45-9
- Molecular formula:C13H7F17O2
- Molecular Weight:518.17
![1-Iodo-1H,1H,2H,2H-perfluorodecane](/CAS/GIF/2043-53-0.gif)
2043-53-0
197 suppliers
$9.00/5g
![POTASSIUM ACRYLATE](/CAS/GIF/10192-85-5.gif)
10192-85-5
103 suppliers
$7.00/5g
![1H,1H,2H,2H-Heptadecafluorodecyl acrylate](/CAS/GIF/27905-45-9.gif)
27905-45-9
226 suppliers
$11.00/2g
Yield:27905-45-9 99%
Reaction Conditions:
with 4-methoxy-phenol;hydroquinone in tert-butyl alcohol at 180; for 6 h;Conversion of starting material;
Steps:
6 Example 6
The catalyst was separated from the reaction liquid obtained in Example 5 by filtration, and the unreacted olefin was removed with an evaporator, giving 47.5 g of solid CF3(CF2)7CH2CH2I. A 200-ml SUS autoclave was charged with 47.5 g (0.082 mol) of the obtained solid CF3(CF2)7CH2CH2I, 9.9g (0.090 mol) of potassium acrylate, 25 g of t-butanol (solvent), 0.6 g of hydroquinone (polymerization inhibitor) and 0.01 g of hydroquinone monomethyl ether (polymerization inhibitor), and a reaction was then carried out with stirring at 180°C for 6 hours.. As a result, CF3(CF2)7CH2CH2OCOCH=CH2 was obtained at a CF3(CF2)7CH2CH2I conversion rate of 99% and at a selectivity of 88%.. The results of NMR analysis revealed that polymerization of CF3(CF2)7CH2CH2OCOCH=CH2 was not detected.
References:
EP1457477,2004,A1 Location in patent:Page column 8
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![POTASSIUM ACRYLATE](/CAS/GIF/10192-85-5.gif)
10192-85-5
103 suppliers
$7.00/5g
![1H,1H,2H,2H-Heptadecafluorodecyl acrylate](/CAS/GIF/27905-45-9.gif)
27905-45-9
226 suppliers
$11.00/2g
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226 suppliers
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30389-25-4
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$15.00/250mg
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678-39-7
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$10.00/1g
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704 suppliers
$20.50/500ml
![1H,1H,2H,2H-Heptadecafluorodecyl acrylate](/CAS/GIF/27905-45-9.gif)
27905-45-9
226 suppliers
$11.00/2g
![2-(Perfluorodecyl)ethyl acrylate](/CAS/GIF/17741-60-5.gif)
17741-60-5
98 suppliers
$35.00/5g