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Gemini quaternary ammonium salt or quaternary ammonium salt compound and preparation method
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A kind of technology of gemini quaternary ammonium salt and compound
Active Publication Date: 2017-04-26
CHINA PETROLEUM & CHEM CORP +1
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Problems solved by technology
[0007] One of the technical problems to be solved by the present invention is the problem of poor template skeleton rigidity and poor orientation in the prior art, and a new type of gemini quaternary ammonium salt or quaternary ammonium base compound is provided
Method used
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Embodiment 1
[0028]
[0029] Dissolve 52.8 grams of 1,4-dibenzyl bromide in 500 milliliters of ethanol, add 60.7 grams of N-methylmorpholine, raise the temperature to 60°C, stir for 8 hours, stop the reaction and filter, and filter the cake with 100 milliliters of ethyl acetate , washed three times with 100 ml of ether to obtain 90.6 g of Geminiquat 1. 1 H NMR (400MHz, DMSO-D 6 )δ7.69(s,4H),4.76(s,4H),4.35(s,2H),3.59-3.53(m,8H),3.61-3.51(m,4H),3.50-3.39(m,2H) ,3.09(s,6H).
Embodiment 2
[0031]
[0032] Dissolve 5.96 g of 2-chloro-1,4-p-dibenzyl bromide in 100 ml of ethanol, add 8.1 g of N-methylmorpholine, raise the temperature to 60°C, stir for 10 hours, stop the reaction and filter, and filter the cake with 20 mL of ethyl acetate, washed three times with 20 mL of ether to obtain 9.05 g of Gemini quaternary ammonium salt 2. 1 H NMR (400MHz, DMSO-D 6 )δ7.60(s,1H),7.34(d,J=7.5Hz,1H),7.08(d,J=7.5Hz,1H),4.70(s,4H),4.29(s,2H),3.61- 3.50(m,8H),3.60-3.53(m,4H),3.51-3.37(m,2H),3.05(s,6H).
Embodiment 3
[0034]
[0035] Dissolve 5.28 grams of 1,4-dibenzyl bromide in 100 milliliters of ethanol, add 9.22 grams of N-ethylmorpholine, raise the temperature to 60°C, stir for 16 hours, stop the reaction and filter, and filter the cake with 20 milliliters of ethyl acetate , washed three times with 20 ml of diethyl ether to obtain 10.04 g of Gemini quaternary ammonium salt 3. 1 H NMR (400MHz, DMSO-D 6 )δ7.40(s,1H),4.70(s,4H),4.29(s,2H),3.55-3.40(m,8H),3.60-3.53(m,4H),3.51-3.37(m,2H) ,3.15(q,J=8.0Hz,4H),1.25(t,J=8.0Hz,6H).
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Abstract
The invention relates to gemini quaternaryammonium salt or a quaternaryammonium salt compound and a preparation method. The technical problems that a template existing in the prior art is poor in framework rigidity and poor in guidance quality are mainly solved. According to the technical scheme, gemini quaternaryammonium salt or the quaternary ammonium salt compound is adopted, and the structure is shown as the following structure general formula, wherein R1 is alkyl of C1-C10, R2 is at least one of H, halogen and alkyl of C1-C6, and X is any one of chlorine, bromine, iodine and hydroxyl, and the problem is solved well. Gemini quaternary ammonium salt or the quaternary ammonium salt compound is high in structural rigidity and can serve as a template to be used for synthesis of a zeolitemolecular sieve. The general formula is shown in the specification.
Description
technical field [0001] The invention relates to a gemini quaternary ammonium salt or quaternary ammonium base compound and a preparation method. Background technique [0002] Quaternary ammonium salts, also known as quaternary ammonium salts, are compounds in which all four hydrogen atoms of ammonium ions are replaced by alkyl groups. Most of the anion groups are halogen anions, which are obtained when halogen anions are exchanged for hydroxide ions Molecules are called quaternary amine bases. [0003] Quaternary ammonium salt molecules have many uses, and generally can be used as: bactericidal disinfectant, soft antistatic agent, flocculant, demulsifier, drag reducer, thickener, anionic synergist, etc. Quaternary ammonium salts that exist in nature generally have biological activity, and some quaternary ammonium salts can be used as phase transfer catalysts for medicinal purposes, pesticides, and chemical reactions. Quaternary ammonium salts are a broad class of cationic ...
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