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REACTION PRODUCTS OF ANILINES WITH BISPHENOLIC EISES OF BISPHENOL A PROCESS FOR THEIR PREPARATION AND THEIR USE AS HARDNESS ACCELERATORS
REACTION PRODUCTS OF ANILINES WITH BISPHENOLIC EISES OF BISPHENOL A PROCESS FOR THEIR PREPARATION AND THEIR USE AS HARDNESS ACCELERATORS
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机译:苯胺与双酚的双酚反应产物及其制备和用作硬性促进剂的方法
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Cpds. of formula (I) are new, where A = -(p-phenylene)-CR4R5-(p-phenylene)-; R1 = 1-6C alkyl or cycloalkyl, opt. with inert substits., and R1 is Et if n = 0; R2, R3 = H, 1-6C alkyl or cycloalkyl, or halo, and R2 is Me if R3 is H, and R3 is Me if R2 is H; R4, R5 = Me, or R4 + R5 may form an opt. substd. cyclohexane ring together with the C atom between the aromatic rings; R6, R7 = as for R2, R3, but with (cyclo)alkyl gps. opt. contg. inert substits.; m = 1-3; n = 0-2; both m, n may be whole nos. or fractions (statistical average). Also claimed is prepn. of (I) by reacting an amine of formula (II) with a diepoxide of formula (III) in a mole ratio of (II):(III) = (1.25:1)-(2:1) at 100-250 degrees C. In the formulae R1-R7, n = as before; A = -(p-phenylene)-CR4R5-(p-phenylene)-; and p = 0-2 (whole no. or fraction as above).
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机译:Cpds。式(I)的通式是新的,其中A =-(对亚苯基)-CR 4 R 5-(对亚苯基)-; R1 = 1-6C烷基或环烷基,最佳。如果n = 0,则R1为Et; R2,R3 = H,1-6C烷基或环烷基,或卤素,并且如果R3为H,则R2为Me,如果R2为H,则R3为Me; R4,R5 = Me或R4 + R5可能构成选择。取代环己烷环与芳环之间的C原子一起; R 6,R 7 =与R 2,R 3相同,但具有(环)烷基gps。选择。续惰性替代品。 m = 1-3; n = 0-2; m,n可能都是整数。或分数(统计平均值)。还声称是prepn。通过使式(II)的胺与式(III)的二环氧化合物以(II):( III)=(1.25:1)-(2:1)的摩尔比在100-250度下反应来制备(I) C.在式R1-R7中,n =如前; A =-(对亚苯基)-CR4R5-(对亚苯基)-; p = 0-2(全数或小数同上)。
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