2-site ethynyl contained pyrimidine ring liquid crystal compounds and method for preparing the same
A technology of liquid crystal compounds and pyrimidine rings, used in chemical instruments and methods, liquid crystal materials, organic chemistry, etc., can solve the problems of unsatisfactory users of liquid crystal materials and unsuitable performance, and improve low-temperature miscibility, large Electrical anisotropy, effect of improving driving voltage
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Embodiment 1
[0061] The liquid crystal compound described in the present embodiment is 2-(4'-pentylphenylacetylene)-5-propylpyrimidine, and its chemical formula (I-1) is as follows:
[0062]
[0063] Its preparation method is:
[0064] The preparation of step 1,2-hydroxy-5-propylpyrimidine:
[0065] Add 64g (0.45mol) of α-propyl-β-ethoxyacrolein, 20g of urea and 200ml of methanol into the reaction flask, control the temperature at 10-20°C, feed 0.2 mole of HCL gas, and react for 5-6 hours , then heated to reflux for 4 hours, then lowered the temperature, decompressed, and removed the organic solvent to obtain an oily solid, which was recrystallized with 3 times of ethanol, then filtered, and the filter cake was washed with 20ml of cold ethanol to obtain light white 2- 33.1 g of hydroxy-5-propylpyrimidine crystals, the gas chromatography purity of this product is ≥99.5%, and the yield is 75%.
[0066] The preparation of step 2, 2-chloro-5-propylpyrimidine:
[0067] Add 44.6g (0.32mol)...
Embodiment 2
[0073] The liquid crystal compound described in the present embodiment is 2-(4'-methoxyphenylacetylene)-5-propylpyrimidine, and its chemical formula (formula I-2) is as follows:
[0074]
[0075] The preparation process is the same as that of Example 1, except that in step 3, the raw material used in this example is 4-methoxyphenylacetylene instead of 4-pentylphenylacetylene.
[0076] Prepare the performance experiment result of compound (I-2) as follows:
[0077] Phase change of liquid crystal compound: C75.3°C N81.3°CI.
Embodiment 3
[0079] The liquid crystal compound described in the present embodiment is 2-(2'-fluoro-4'-pentylphenylacetylene)-5-propylpyrimidine, and its chemical formula (formula I-3) is as follows:
[0080]
[0081] Its preparation process is the same as in Example 1, except that the raw material 4-pentylphenylacetylene in step 3 of Example 1 is changed to 2-fluoro-4-pentylphenylacetylene to prepare the target product (I-3) .
[0082] It is known through experiments that the phase change of this liquid crystal compound is: C52.5°C N67.5°CI.
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