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ChemicalBook CAS DataBase List hexafluorobenzene
392-56-3

hexafluorobenzene synthesis

6synthesis methods
The direct synthesis of hexafluorobenzene from benzene and fluorine is not possible. The synthetic route proceeds via the reaction of alkali-fluorides with halogenated benzene:
C6Cl6 + 6 KF → C6F6 + 6 KCl
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Yield:392-56-3 71.7%

Reaction Conditions:

with sulfolane;potassium fluoride;tetrakis(diethylamino)phosphonium bromide in nitrobenzene;toluene at 120 - 240; for 30 h;Inert atmosphere;Autoclave;Reagent/catalyst;Temperature;

Steps:

2 Example 2
In a 1000 ml four-necked flask equipped with a water separator, 134 g of potassium fluoride, 350 ml of sulforan and 300 ml of toluene were successively added. After stirring under mechanical stirring, the mixture was heated to 120-130°C under reflux, and the water was separated. After no water was removed, the water separator was turned on and the heat was removed to remove the toluene at 185°C. When no toluene was distilled off, the nitrogen protection was allowed to cool to room temperature, transferred to a 1000 ml autoclave, 314 g of chloropentafluorobenzene, 15 g of tetrakis(diethylamino)phosphonium bromide, and 5 g of nitrobenzene were added, and the temperature was raised to 240°C for 30 hours. . After the reaction was completed, the reaction system was distilled at atmospheric pressure and received a fraction of 40 to 160°C. The above-mentioned receiver was subjected to atmospheric rectification using a 30 cm packed distillation column, and at the same time, a 79-81° C. fraction was received to obtain a final product with a purity of more than 99%. The yield was 71.7%.

References:

Dalian Qikai Pharmaceutical Technology Co., Ltd.;Tian Hanqing;Jiang Dianping;Zhang Hongxue CN107827704, 2018, A Location in patent:Paragraph 0024-0031

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