Compound, method for producing same, resin composition, resin sheet, multilayer printed wiring board, and semiconductor device
A technology of resin composition and compound, which is applied in the field of compound and can solve problems such as long processing time
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[0372] Hereinafter, the present embodiment will be described more specifically with reference to Examples and Comparative Examples. This embodiment is not limited to the following examples at all.
[0373] [Synthesis of maleimide compound (TMDM)]
Synthetic example 1
[0375] The compound (TMDM) represented by (21) was synthesized by the following formula.
[0376] [Synthesis of amic acid compound (hereinafter, abbreviated as MA-TMDA)]
[0377] First, MA-TMDA represented by the formula (33) was synthesized by the following method.
[0378]
[0379] In a 100 mL four-necked flask equipped with an argon blowing inlet, a Dean-Stark trap, a serpentine condenser, and a thermometer, 5.2 g (53 mmol) of maleic anhydride, N-methylpyrrolidone (NMP ) 20 mL and 20 mL of toluene were stirred at room temperature (25° C.) under argon gas flow to completely dissolve maleic anhydride. To this solution, TMDA (manufactured by Junya Pharmaceutical Co., Ltd., 5-amino-1,3,3-trimethyl-1-(4-aminophenyl)-indane and 6-amino-1,3, 3-trimethyl-1-(4-aminophenyl)-indane mixture) 5.0 g (19 mmol) and NMP 10 mL were stirred at room temperature (25° C.) for 17 hours.
[0380] A part of the reaction solution was fractionated, water and ethyl acetate were added, and the mi...
Embodiment 1
[0390] The compound represented by formula (16) (also referred to as compound (A-1)) was synthesized as follows.
[0391] In a 200 mL flask, 6.56 g (55.5 mmol) of 1,10-decanediol (manufactured by Tokyo Chemical Industry Co., Ltd.), cyclohexane-1,2,4-tricarboxylic acid-1,2-anhydride (Mitsubishi Chemical Industries, Ltd.) were added. Gas Chemical Co., Ltd., H-TMAn (trade name) 23.10 g (116.6 mmol), 4-dimethylaminopyridine 6.77 g (55.5 mmol), triethylamine 12.35 g and dichloromethane 60 g, at room temperature (25 °C) under stirring for 7 hours.
[0392] To the reaction solution, 100 mL of water and 50 mL of dichloromethane were added, and the mixture was further stirred for 1 hour. Further, 150 mL of dichloromethane and 50 mL of 1M hydrochloric acid were added for liquid separation, and the aqueous layer was removed. To the obtained organic layer, 60 mL of 1M hydrochloric acid was added and stirred. After liquid separation and removal of the aqueous layer, the mixture was wash...
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