A self-alignment additive and a preparation method and application thereof
An additive and self-alignment technology, applied in chemical instruments and methods, optics, instruments, etc., can solve problems such as time-consuming, weak anchoring ability of liquid crystal molecules, and application limitations
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Embodiment 1
[0081] Synthesis of Embodiment 1 BYLC-01
[0082] The structural formula of the liquid crystal compound is:
[0083]
[0084] The synthetic route for preparing compound BYLC-01 is as follows:
[0085]
[0086] Specific steps are as follows:
[0087] (1) Synthesis of compound BYLC-01-1:
[0088] Under the protection of nitrogen, add 40.0g of p-bromoanisole and 280ml of tetrahydrofuran to the reaction flask, and add 0.26mol of n-butyllithium n-hexane solution dropwise at -70~-80°C under temperature control.
[0089] 32.0 g of trimethyl borate was added dropwise at -60 to -70°C under temperature control, and then returned to -30°C naturally.
[0090] Add 400 ml of 2M hydrochloric acid aqueous solution for acidification, perform conventional post-treatment, and recrystallize petroleum ether to obtain 28.3 g of light yellow solid (compound BYLC-01-1), HPLC: 99.7%, yield: 85.7%.
[0091] (2) Synthesis of compound BYLC-01-2:
[0092] Under nitrogen protection, 28.3g of com...
Embodiment 2
[0098] According to the technical scheme of Example 1, the following compounds can be synthesized by simply replacing the corresponding raw materials without changing any substantive operations:
[0099]
[0100]
[0101] R represents a hydrogen atom or an alkyl group with 1-5 carbon atoms, wherein, one or more non-adjacent CH 2 The radicals can be replaced independently of each other by -O- not directly connected to each other; n represents 0, 1, 2, 3, 4 or 5.
Embodiment 3
[0102] Synthesis of Embodiment 3 BYLC-02
[0103] The structural formula of the liquid crystal compound is:
[0104]
[0105] The synthetic route for preparing compound BYLC-02 is as follows:
[0106]
[0107] Specific steps are as follows:
[0108] (1) Synthesis of compound BYLC-02-1:
[0109] Add 50.0 g of p-bromoanisole and 450 ml of tetrahydrofuran to the reaction flask, add dropwise 0.315 mol of n-butyl lithium in n-hexane solution at -70 to -80°C under temperature control, and react for 1 hour under temperature control;
[0110] A solution consisting of 46.0 g of 4-(3-ethylcyclopentyl) cyclohexanone and 150 ml of tetrahydrofuran was added dropwise at a temperature of -70 to -80°C, and then the temperature was naturally returned to -30°C.
[0111] Add 500ml of 2M hydrochloric acid aqueous solution for acidification and conventional post-treatment to obtain 76.2g of light yellow liquid (compound BYLC-02-1), GC: 93.8% (cis + trans), yield: 96.4%.
[0112](2) Synth...
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