Diamine compound, method for preparing same, liquid crystal alignment agent, liquid crystal alignment film, and liquid crystal display device
A technology of liquid crystal alignment agent and amine compound, applied in the field of new structure diamine compound and its preparation, can solve the problems such as inability to solve the problem by rubbing method, uneven alignment fixing force and inclination angle, poor economical efficiency of optical pattern forming process, etc. , to achieve the effect of ensuring safety and economy
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preparation example Construction
[0066] The preparation method of the diamine compound represented by the chemical formula 10 includes the following steps:
[0067] Reacting a compound represented by the following Chemical Formula 6 with a compound represented by the following Chemical Formula 8 to prepare a compound represented by the following Chemical Formula 9; and
[0068] Removing the protecting group PG of the compound represented by the following chemical formula 9;
[0069] [Chemical formula 6]
[0070]
[0071] [Chemical formula 8]
[0072]
[0073] [Chemical formula 9]
[0074]
[0075] [Chemical formula 10]
[0076]
[0077] In the chemical formulae 6, 8, 9 and 10, n is an integer from 1 to 20; R 1 To R 8 It is the same or different, and each independently represents H, CN, NO2, CF3, halogen, an alkyl group having 1 to 10 carbon atoms, or an alkoxy group having 1 to 10 carbon atoms; PG is benzyloxycarbonyl (Carbobenzyloxy, Cbz), p-Methoxybenzyl carbonyl (Moz), tert-butyloxycarbonyl (tert-butyloxycarbonyl, BO...
preparation Embodiment 1
[0200] Preparation of chemical formula 10 (n=1, R 1 ~R 8 =H, PG=BOC) compound
[0201] [Reaction formula I]
[0202]
[0203] Dissolve 95.0g (0.74mol) of the raw material 4,4,4-trifluorobutan-1-ol (chemical formula 1) in 135ml (0.97mol) of triethylamine (TEA) and 1L of dichloromethane (Methylene Chloride, MC) and cooled to 0°C. Within 30 minutes, slowly add 63.0ml (62.0ml) of methanesulfonyl chloride (MsCl) to the resulting substance. The mixture was stirred at 0°C for 10 minutes and allowed to react at room temperature for 2 hours to prepare 4,4,4-trifluorobutyl methanesulfonate (Chemical Formula 2) ).
[0204] The results of NMR detection of the compound of Chemical Formula 2 are as follows.
[0205] 1 H NMR (400MHz, CDCl 3 ) Δ4.30 (t, 2H), 3.04 (s, 3H), 2.28 (m, 2H), 2.05 (m, 2H)
[0206] [Reaction formula Ⅱ]
[0207]
[0208] Next, 75.9g (0.56mol) of 4-hydroxyacetophenone (chemical formula 3), 55.2g (0.84mol) of KOH, 146g (0.61mol) of chemical formula 2 methanesulfonic aci...
preparation Embodiment 2
[0227] Preparation of compound of chemical formula 23 (when n=1, R1~R8=H, PG=BOC)
[0228] [Reaction formula Ⅵ]
[0229]
[0230] Dissolve 95.0 (0.74mol) of the raw material 4,4,4-trifluorobutan-1-ol (chemical formula 1) in 135ml (0.97mol) of triethylamine and 1L of dichloromethane, and within 30 minutes Slowly add 63.0ml (0.81mol) of methanesulfonyl chloride (MsCl) at 0°C. The mixture was stirred at 0°C for 10 minutes, and reacted at room temperature for 2 hours to prepare 4,4,4-trifluorobutyl methanesulfonate (Chemical Formula 2).
[0231] The results of NMR detection of the compound of Chemical Formula 2 are as follows.
[0232] 1 H NMR (400MHz, CDCl 3 ) Δ4.30 (t, 2H), 3.04 (s, 3H), 2.28 (m, 2H), 2.05 (m, 2H)
[0233] [Reaction formula Ⅶ]
[0234]
[0235] Dissolve 72.5g (0.53mol) of 4-hydroxyacetophenone (chemical formula 3) in 700mL of DMF and mix it with 152g (0.64mol) of methanesulfonic acid 4 prepared by reaction formula VI. 4,4-trifluorobutyl methanesulfonate (chemical formu...
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