Spontaneous combustion ionic liquid containing tension ring structure and application
An ionic liquid and tension technology, used in organic chemistry, explosives, etc., can solve the problems of human and environmental hazards, low density specific impulse of non-hydrazine materials, and high toxicity.
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Embodiment 1
[0028] The preparation of ionic liquid, the steps are as follows:
[0029] 1-Methylcyclopropyl-3-methylimidazolium dicyanoammonium salt:
[0030] In the first step, imidazole (6.808g, 0.100mol) and sodium hydroxide (8.000g, 0.200mol) were added to a 500ml round-bottomed flask, and the reaction was vigorously stirred at 90 °C for 5 hours, and then dried in a vacuum oven.
[0031] In the second step, methylcyclopropyl bromide (9.450 g, 0.070 mol) was added to the dried product, and 200 ml of THF was added, and the reaction was vigorously stirred at 40 °C for 40 hours. After the reaction is completed, filter, and wash the solid with 10% of the original volume of THF, combine the filtrates, and finally evaporate the solvent, add 100 ml of deionized water and 100 ml of dichloromethane for extraction, and obtain an organic phase. Dichloromethane is evaporated to obtain a methyl ring propylimidazole.
[0032] In the third step, methylcyclopropylimidazole (12.200g, 0.100mol) and met...
Embodiment 2
[0035] The preparation of ionic liquid, the steps are as follows:
[0036] 1-Methylcyclobutyl-3-propylimidazolium dicyanoammonium salt:
[0037] In the first step, imidazole (6.808 g, 0.100 mol) and sodium hydroxide (4.800 g, 0.120 mol) were added to a 500 ml round-bottomed flask, and the reaction was vigorously stirred at 110 °C for 3 hours, and then dried.
[0038] In the second step, methylcyclobutyl bromide (16.390 g, 0.110 mol) was added to the dried product, and 100 ml of THF was added, and the reaction was vigorously stirred at 50 °C for 20 hours. After the reaction is completed, filter, and wash the solid with 10% of the original volume of THF, finally evaporate the solvent, add 50 ml of deionized water and 50 ml of dichloromethane for extraction, obtain an organic phase, and steam out the dichloromethane to obtain methylcyclopropylimidazole .
[0039] In the third step, methylcyclobutylimidazole (13.600g, 0.100mol) and iodopropane (18.699g, 0.110mol) were added to a 1...
Embodiment 3
[0042] The preparation of ionic liquid, the steps are as follows:
[0043] 1-Cyclobutyl-3-pentylimidazolium dicyanoammonium salt:
[0044] In the first step, imidazole (6.808 g, 0.100 mol) and sodium hydroxide (4.000 g, 0.100 mol) were added to a 500 ml round-bottomed flask, and the reaction was vigorously stirred at 120 °C for 2 hours, and then dried.
[0045] In the second step, cyclobutyl bromide (20.250 g, 0.150 mol) was added to the dried product, and 80 ml of acetonitrile was added, and the reaction was vigorously stirred at 80 °C for 10 hours. After the reaction is completed, filter, and wash the solid with 10% of the original volume of acetonitrile, finally evaporate the solvent, add 50 ml of deionized water and 50 ml of dichloromethane for extraction, obtain an organic phase, and steam out the dichloromethane to obtain methylcyclopropylimidazole .
[0046] The third step is to take cyclobutylimidazole (12.200g, 0.100mol) and iodopentane (29.708g, 0.150mol) into a 10...
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