A kind of furan ring side group-containing triazine polyurethane char-forming agent and its synthesis method
A synthesis method and triazine technology are applied in the field of triazine polyurethane carbon-forming agent and its synthesis, and achieve the effects of less side reactions, improved degradability, and easy operation.
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Embodiment 1
[0042] In a 1000mL three-necked flask, completely dissolve 1mol cyanuric chloride in 300mL1,4-dioxane, under ice-salt bath and nitrogen protection, dissolve 100mL1 of 1mol furfurylamine and 1mol triethylamine, The 4-dioxane solution was slowly dropped into it, and the dropping time was controlled to be 2 hours. After the dropping was completed, the reaction was continued for 2 hours in an ice-salt bath.
[0043] At room temperature, 100 mL of 1,4-dioxane solution dissolved with 2 mol of ethylenediamine and 2 mol of triethylamine was slowly dropped into it, and after the addition, the temperature was raised to 110° C. to continue the reaction for 8 hours. After the reaction was completed, suction filtration was performed, and the filtrate was rotary evaporated to obtain a solid powder, which was washed with deionized water for 5 times, and product 1 was obtained after vacuum drying, which was set aside.
[0044] Dissolve 1 mol of product 1 completely dehydrated and 1 mol of 4,4...
Embodiment 2
[0047] In a 1000mL three-necked flask, completely dissolve 1mol of cyanuric chloride in 400mL of acetonitrile, and slowly drop 100mL of acetonitrile solution dissolved in 1mol of methylfurylamine and 1mol of pyridine into it under ice-salt bath and nitrogen protection. Adding time is 2h. After the dropwise addition, continue to react in ice-salt bath for 2h.
[0048] At room temperature, 100 mL of acetonitrile solution dissolved with 2 mol of phenolphthalein and 2.6 mol of pyridine was slowly dropped into it, and after the addition was completed, the temperature was raised to 110° C. to continue the reaction for 8 h. After the reaction, filter with suction, spin evaporate the filtrate to obtain a solid powder, wash with deionized water for 5 times, and dry in vacuum to obtain the product 2, which is set aside.
[0049] Dissolve 1 mol of product 2 completely dehydrated and 1 mol of hexamethylene diisocyanate (HDI) in 400 mL of toluene dehydrated, mechanically stir evenly, add 2...
Embodiment 3
[0052] In a 1000mL three-necked flask, completely dissolve 1mol of cyanuric chloride in 300mL of 1,4-dioxane; The oxane solution was slowly dropped into it, and the dropping time was controlled to be 2h. After the dropping was completed, the reaction was continued for 2h in an ice-salt bath.
[0053] At room temperature, 100 mL of 1,4-dioxane solution dissolved with 2 mol of 4,4-diaminodiphenylmethane (DDM) and 2 mol of pyridine was slowly dropped into it. After the addition was completed, the temperature was raised to 110° C. to continue the reaction for 8 h. After the reaction, suction filtration was performed, and the filtrate was rotary evaporated to obtain a solid powder, which was washed with deionized water for 5 times, and the product 3 was obtained after vacuum drying, which was set aside.
[0054] Dissolve 1 mol of product 3 completely dehydrated and 1 mol of isophorone diisocyanate (IPDI) in 500 mL of N,N-dimethylformamide dehydrated, mechanically stir evenly, add 2...
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