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HRID 1701464作成日:2026年10月26日

Toluene → bis(3,5-Dimethylcyclohexyl)phthalate

https://huagongshe.com/reaction/1701464

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Phthalic AnhydrideHCID 6811—
反応物3,5-Dimethylcyclohexan-1-olHCID 21584—
溶媒WaterHCID 962—
生成物bis(3,5-Dimethylcyclohexyl)phthalateHCID 20751009—

反応手順

100 ml of toluene was added to a mixture of 44.4 g (0.3 mol) of phthalic anhydride, 83.3 g (0.66 mol) of 3,5-dimethylcyclohexanol and 2 g of p-toluenesulfonic acid and the mixture was refluxed with heating for 12 hours with the azeotropic removal of 6 ml of water. After the reaction, the mixture was cooled and 200 ml of toluene was added to the mixture. The organic solvent layer was washed with water, a 5% aqueous solution of sodium hydroxide and water, in this order and dried with anhydrous sodium sulfate. After filtering the mixture, the filtrate was concentrated under reduced pressure. 50 ml of hexane was added to the concentrate and column chromatographed to obtain the desired compound. The carrier used was 800 g of Silica Gel 60 manufactured by Merck Co. Hexane and hexane-diethyl ether (9:1 in volume ratio) were used as the solvent and 105.7 g (yield 91.2%) of Compound (5) was obtained from the hexane-diethyl ether eluate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04193802
出典データセットuspto-grants-1980_03
ORD IDord-30b75737d8764cd18a84186f1e117dd2
出典メモuspto-grants-1980_03