Polyamideimide having norbornane skeleton and production method for same
A technology of polyamideimide and norbornane, applied in the field of polyamideimide, can solve the problems of lack of transparency and easy coloring, and achieve the effects of excellent transparency and excellent heat resistance
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[0156] Hereinafter, the present invention will be described in detail through examples. However, the scope of the present invention is not limited to the following examples.
[0157]
Synthetic example 1)
[0158] (Synthesis Example 1) [Formation of Cyclopentadiene]
[0159] [chemical 14]
[0160]
[0161] 700 g of dicyclopentadiene was charged into a 1-liter flask equipped with a stirrer, a thermometer, and a Schneider-type fractionating tube (7 stages) equipped with a fractionating column, a thermometer, and a cooling tube on the top of the column, and heated in an oil bath. When the temperature in the flask reached 158° C., cyclopentadiene was gradually distilled from the top of the fractionation column, and therefore, it was recovered in about 6 hours while cooling the receiver with ice. The distillation temperature at this time was 41-48 degreeC, and the recovery amount was 609g (recovery rate: 87%). The resulting cyclopentadiene was analyzed by gas chromatography, and the result was a purity of 100%.
Synthetic example 2)
[0162] (Synthesis example 2) [Synthesis of norbornene dicarboxylate methyl ester]
[0163] [chemical 15]
[0164]
[0165] In a 1-liter flask with a stirrer, a thermometer, a dropping funnel, and a cooling tube, drop 432 g (3.0 moles) of dimethyl maleate, cool the flask with water, and add dropwise the ring obtained in Synthesis Example 1 while stirring. 198g (3.0 moles) of pentadiene, while keeping the temperature in the flask at 30-40°C. After completion of the dropwise addition, the reaction was carried out for 6 hours while maintaining the reaction temperature, and analyzed by a gas chromatograph. As a result, dimethyl maleate and cyclopentadiene as raw materials completely disappeared, and methyl norbornene dicarboxylate was obtained. The reaction solution with a selectivity of 99.2% (0.8% of dicyclopentadiene formation). In addition, the isomer ratio of this norbornene dicarboxylate methyl ester was exo isomer / endo isomer=25 / 75.
[0166]
PUM
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