FIELD: chemistry.
SUBSTANCE: present invention relates to a process for the preparation of hydrophobically associating macromonomers of M and novel macromonomers. Described is a process for the preparation of a macromonomer M of general formula (I) H2C=C(R1)-R2-O-(-CH2-CH2-O-)k-(-CH2-CH(R3)-O-)l-(-(-CH2-CH2-O-)m-R4 (I), wherein structural units (-CH2-CH2-O-)k and (-CH2-CH(R3)-O-)l and optionally -(-CH2-CH2-O-)m in the block structure are located in the sequence represented in formula (I) wherein the residues and indices have the following values: k is a number from 10 to 150; l is a number from 5 to 25; m is a number from 0 to 15; R1 is H; R2 independently of each other, is a divalent linking group -O-(Cn'H2n')-, where n' is a natural number from 3 to 5; R3 independently of one another, is a hydrocarbon radical having 2 to 14 carbon atoms, with the proviso that the total number of carbon atoms in all hydrocarbon residues R3 is in the range from 15 to 50; R4 is H, which includes the following steps: a) reacting monoethylenically unsaturated alcohol A1 of general formula (II) H2C=C(R1)-R2-OH (II), with ethylene oxide, wherein radicals R1 and R2 have values given above; with the addition of alkaline catalyst K1 containing KOMe and/or NaOMe; wherein alkoxylated alcohol A2 is obtained; b) reacting alkoxylated alcohol A2 with at least one alkylene oxide Z of formulae (Z), where R3 has the above value; with addition of alkaline catalyst K2, wherein catalyst K2 comprises at least one basic sodium compound selected from NaOH, NaOMe and NaOEt; wherein the potassium ion concentration during the reaction in step b) is less than or equal to 0.9 mol% relative to alcohol A2 used; and wherein the reaction in step b) is carried out at a temperature below or equal to 135°C, wherein alkoxylated alcohol A3 is obtained according to formula (III), H2C=C(R1)-R2-O-(-CH2-CH2-O-)k-(-CH2-CH(R3)-O-)l-R4 (III), where R4=H, where the residues R1, R2 and R3 and indices k and l have the values given above; c) optionally, reacting at least a portion of alkoxylated alcohol A3 with ethylene oxide, wherein alkoxylated alcohol A4 is obtained which corresponds to macromonomer M according to formula (I), wherein R4= H, and m is greater than 0. Macromonomer obtained using said method is also described.
EFFECT: technical result is the production of hydrophobically associating macromonomers having a small number of cross-linking groups and which can be polymerised to produce copolymers with a small amount of gels.
19 cl, 1 tbl, 30 ex
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Authors
Dates
2018-05-11—Published
2013-12-13—Filed