Polyimide-based traction belt
A polyimide-based traction and polyimide resin technology, applied in the field of traction belts, can solve the problems of solvent resistance, poor mechanical properties and environmental adaptability, and low heat resistance level
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Embodiment 1
[0154] (1) Add 69.52g (0.56mol) of 3-methoxyphenol, 88.23g (0.56mol) of p-nitrochlorobenzene, 85.14g (0.616mol) of potassium carbonate and 200g of dimethyl sulfoxide into the reactor in sequence , heated to 160°C and reacted for 6h; cooled to 60°C, added to 2000mL water, precipitated crude product, filtered out, dissolved in dichloromethane after washing, dried over anhydrous magnesium sulfate, concentrated solvent, obtained crude product again, and re- Crystallization obtained 114.23 g of the refined product of compound (II-1) represented by formula (II); the yield was 83.2%.
[0155] Utilize nuclear magnetic resonance to characterize the structural compound (II-1) shown in the formula (II) that obtains, the proton nuclear magnetic resonance spectrum result that obtains is: 1 H NMR (400MHz, DMSO) δ = 8.280–8.205 (m, 2H), 7.389 (t, J = 8.2Hz, 1H), 7.170–7.095 (m, 2H), 6.875 (dd, J = 8.3Hz, 2.2Hz , 1H), 6.776(t, J=2.2Hz, 1H), 6.731(dd, J=8.0Hz, 2.0Hz, 1H), 3.765(s, 3H).
[01...
Embodiment 2
[0163] (1) 62.07g (0.50mol) 3-methoxyphenol, 101.0g (0.50mol) m-bromonitrobenzene, 4.76g (0.025mol) cuprous iodide, 76.02g (0.55mol) potassium carbonate and 200g Add N,N-dimethylformamide to the reaction flask in turn, heat the reaction system to 150°C for 12 hours under the protection of nitrogen, and react for 12 hours; after cooling to 60°C, add it to 2000mL water, precipitate the crude product, filter it out, wash with water and dissolve Dry in dichloromethane and anhydrous magnesium sulfate, concentrate the solvent, and purify to obtain 90.59 g of the refined product of compound (II-2) represented by formula (II); the yield is 73.9%.
[0164] (2) 89.07g (0.48mol) 4-nitrobenzoyl chloride, 69.34g (0.52mol) aluminum trichloride, 1000mL dichloromethane and 105.45g (0.43mol) structure compound (II) shown in formula (II) -2) Sequentially add to the reactor, stir and react at 20°C for 18h; then slowly add to ice-hydrochloric acid for treatment, separate liquid, dry over anhydrou...
Embodiment 3
[0168] (1) Refer to Step (1) of Preliminary Example 2 to obtain the refined product of compound (II-2) shown in formula (II).
[0169] (2) 18.56g (0.1mol) 3-nitrobenzoyl chloride, 14.67g (0.11mol) aluminum trichloride, 250g 1,2-dichloroethane and 22.07g (0.09mol) formula (II) Compounds (II-2) showing the structure were sequentially added into the reactor, stirred and reacted at 20°C for 30 h; then slowly added to ice-hydrochloric acid for treatment, liquid separation, drying over anhydrous magnesium sulfate, and concentration of the solvent to obtain a crude product. Recrystallization obtained 22.98 g of refined product of compound (III-4) represented by formula (III); the yield was 64.7%.
[0170](3) 39.43g (0.1mol) of the structural compound (III-4) shown in formula (III), 101.15g (40%, 0.5mol) of hydrobromic acid and 350g of acetic acid were added to the reactor successively, at 100°C Stir the reaction for 48 hours; concentrate and recover hydrobromic acid and acetic acid,...
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