![14548-74-4](/CAS/GIF/14548-74-4.gif)
1H,1H-2,5-DI(TRIFLUOROMETHYL)-3,6-DIOXAUNDECAFLUORONONANOL synthesis
- Product Name:1H,1H-2,5-DI(TRIFLUOROMETHYL)-3,6-DIOXAUNDECAFLUORONONANOL
- CAS Number:14548-74-4
- Molecular formula:C9H3F17O3
- Molecular Weight:482.09
![2,5-BIS(TRIFLUOROMETHYL)-3,6-DIOXAUNDECAFLUORONONANOYL FLUORIDE](/CAS/GIF/2641-34-1.gif)
2641-34-1
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$45.00/1 g
![1H,1H-2,5-DI(TRIFLUOROMETHYL)-3,6-DIOXAUNDECAFLUORONONANOL](/CAS/GIF/14548-74-4.gif)
14548-74-4
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$40.00/1 g
Yield:14548-74-4 90%
Reaction Conditions:
with lithium aluminium tetrahydride in diethyl ether at 20; for 2 h;Inert atmosphere;Reflux;
Steps:
1 Example 1
Approximately 1000 mL of water-free water (22.8 g, 0.6 mol) is placed in a 5 L dry bottle, under N2 protection, stirring and dropping hexane (250 g, 0.5 mol), Discharge, drop acceleration is maintainedAfter completion of the addition, stir at room temperature for 2 minutes.5 mL of Bulonic Acid500g ice water, re-join when release6N sulfuric acid oxidation for subsequent use,After the separation, the aqueous phase is 50mL x 3Incorporation of organic liquidWater-free sulfuric acid220g of steamed, rich,The yield is 90% and the GC ratio is 98.3%.1H NMR ,Chemistry 4.15: Multiple peaks, special CH2O peak.
References:
Shandong Dongyue Pending Qingneng Materials Co., Ltd.;Shi Dakuo;Feng Wei;Zhang Yongming;Rong Yue;Xu Yelin CN110790715, 2020, A Location in patent:Paragraph 0037-0039
![PERFLUORO(2,5-DIMETHYL-3,6-DIOXANONANOIC) ACID METHYL ESTER](/CAS/GIF/26131-32-8.gif)
26131-32-8
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$29.19/1g
![1H,1H-2,5-DI(TRIFLUOROMETHYL)-3,6-DIOXAUNDECAFLUORONONANOL](/CAS/GIF/14548-74-4.gif)
14548-74-4
43 suppliers
$40.00/1 g
![Methanesulfonic acid, 1,1,1-trifluoro-, 2,3,3,3-tetrafluoro-2-[1,1,2,3,3,3-hexafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propoxy]propyl ester](/CAS/20210111/GIF/1173110-39-8.gif)
1173110-39-8
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![1H,1H-2,5-DI(TRIFLUOROMETHYL)-3,6-DIOXAUNDECAFLUORONONANOL](/CAS/GIF/14548-74-4.gif)
14548-74-4
43 suppliers
$40.00/1 g