![1644-88-8](/CAS/GIF/1644-88-8.gif)
2-(Trifluoromethoxy)nitrobenzene synthesis
- Product Name:2-(Trifluoromethoxy)nitrobenzene
- CAS Number:1644-88-8
- Molecular formula:C7H4F3NO3
- Molecular Weight:207.11
![3-Nitrophenol](/CAS/GIF/554-84-7.gif)
554-84-7
12 suppliers
$12.00/5g
![Antimony trifluoride](/CAS/GIF/7783-56-4.gif)
7783-56-4
150 suppliers
$23.12/5 g
![2-(Trifluoromethoxy)nitrobenzene](/CAS/GIF/1644-88-8.gif)
1644-88-8
121 suppliers
$10.00/1g
Yield: 62%
Reaction Conditions:
antimonypentachloride in tetrachloromethane
Steps:
2 nitrophenyl trifluoromethyl ether
nitrophenyl trifluoromethyl ether Using the same reactor setup as in Example 1, the reactor is charged with 3-nitrophenol (13.9 g, 0.1 mol), anhydrous carbon tetrachloride (38 ml, 0.39 mol), anhydrous antimony trifluoride (53.6 g, 0.3 mol) and a catalytic amount of antimony pentachloride (1 ml, 7.7 mmol). The reactor is then sealed and heated at 150° C (internal) with vigorous stirring for 5.5 hours. Subsequently, the reactor is opened and the contents neutralized with saturated NaHC03 The product is separated by steam distillation, and a 62 percent yield of the product is obtained.
References:
The Dow Chemical Company US4950802, 1990, A
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100-02-7
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![Antimony trifluoride](/CAS/GIF/7783-56-4.gif)
7783-56-4
150 suppliers
$23.12/5 g
![2-(Trifluoromethoxy)nitrobenzene](/CAS/GIF/1644-88-8.gif)
1644-88-8
121 suppliers
$10.00/1g
![2-(Trifluormethoxy)phenylboronic acid](/CAS/GIF/175676-65-0.gif)
175676-65-0
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![2-(Trifluoromethoxy)nitrobenzene](/CAS/GIF/1644-88-8.gif)
1644-88-8
121 suppliers
$10.00/1g
![BIS(TRIFLUOROMETHYL)PEROXIDE](/CAS/GIF/927-84-4.gif)
927-84-4
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inquiry
![Nitrobenzene](/CAS/GIF/98-95-3.gif)
98-95-3
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![4-(Trifluoromethoxy)nitrobenzene](/CAS/GIF/713-65-5.gif)
713-65-5
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$8.00/1g
![3-(Trifluoromethoxy)nitrobenzene](/CAS/GIF/2995-45-1.gif)
2995-45-1
145 suppliers
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![2-(Trifluoromethoxy)nitrobenzene](/CAS/GIF/1644-88-8.gif)
1644-88-8
121 suppliers
$10.00/1g