Branched polyether alcohol ester compound and application thereof
A technology of ester compounds and branched polyether alcohols, applied in organic chemistry, coating, etc.
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[0021] The method for the compound shown in the preparation formula I provided by the present invention specifically comprises the following steps:
[0022] In the presence of a catalyst (such as p-toluenesulfonic acid, trifluoromethanesulfonic acid, acidic cation exchange resin, solid acid or rare earth Lewis acid, etc.) and an inert gas (such as nitrogen, etc.), the compound shown in formula II and the corresponding of organic carboxylic acids (R 4 COOH or / and R 6 COOH) at 150°C to 170°C for at least 5 hours, cooled and filtered, the filtrate was transferred to a separatory funnel, an appropriate amount of water was added, the water phase was separated, the organic phase was retained, and the organic phase was washed in turn (dissolved with lye and water) After the organic phase is washed to neutrality) and the low boilers are evaporated, the target object (compound shown in formula I) is obtained;
[0023] Wherein, the dosage of the catalyst is 0.05%-0.2% of the total wei...
Embodiment 1
[0029] The preparation of compound shown in formula Ⅰ-1:
[0030]
[0031] 15 grams of polyether polyol (compound shown in formula II-1, technical grade, Shanghai Fujia Fine Chemical Co., Ltd.), 8 grams of isobutyric acid, and 7 grams of anhydrous sodium sulfate are placed in a mechanical stirring and condensation tube, In a four-necked flask with a thermometer, in the presence of 0.1 gram of catalyst (such as p-toluenesulfonic acid, trifluoromethanesulfonic acid, acidic cation exchange resin, solid acid or rare earth Lewis acid, etc.) and nitrogen, the temperature of the reaction system was raised to 150 ℃, and keep stirring at 150℃ for 5h, stop heating, cool down, add appropriate amount of alkylbenzene (such as toluene or xylene, etc.) , the organic phase was washed with lye and water in turn until neutral, and the low boilers were evaporated to obtain a light yellow transparent substance (compound shown in formula Ⅰ-1). The test data of its infrared spectrum is as follo...
Embodiment 2
[0034] The preparation of compound shown in formula Ⅰ-2:
[0035]
[0036] Except that isobutyric acid in Example 1 was replaced by 2-ethyl-hexanoic acid, the other steps and conditions were the same as in Example 1 to obtain a light yellow transparent compound (compound shown in formula I-2). The test data of its infrared spectrum is as follows:
[0037] IR (tablet method): 2968.58 (s, υ-C-H), 1738.79 (s, υ-C=O), 1345.72 (s, υ-C-O-C), 1247.85, 1108.23 (d, υ-CO-O).
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