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HRID 721996作成日:2026年10月26日

Propylene Glycol → 1,2-Propanediol monohydroxytetradecyl ether

https://huagongshe.com/reaction/721996

反応式

関与物質

役割名称HCID仕込み量
反応物Propylene GlycolHCID 1030—
反応物Sulfuric AcidHCID 1118—
反応物1,2-EpoxytetradecaneHCID 18604—
反応物Sodium BicarbonateHCID 516892—
反応物Calcium ChlorideHCID 5284359—
溶媒WaterHCID 962—
生成物1,2-Propanediol monohydroxytetradecyl etherHCID 8790491497.3%

反応条件

温度62.5 °C

反応手順

Separately, a 500 ml mixing vessel equipped with a calcium chloride-containing tube was charged with 318.6 g (1.50 moles) of 1,2-epoxytetradecane. While the charged 1,2-epoxytetradecane was stirred and cooled with water, a concentrated sulfuric acid was gradually dropped in an amount of 2.7 g (0.027 mole) into the cooled 1,2-epoxytetradecane. After stirring for 15 minutes, the resultant mixture was placed into the dropping apparatus attached to the reaction vessel and was dropped into the 1,2-propanediol contained in the reaction vessel and maintained at a temperature of 60 to 65° C. over a time of 2 hours. Then the reaction of the mixture was carried out at a temperature of 60 to 65° C. for one hour. After the exhaustion of the starting material, namely 1,2-epoxytetradecane was confirmed by a thin-layer chromatography, the reaction was stopped. A powdered sodium hydrogen carbonate was mixed in an amount of 2.5 g (0.03 mole) into the resultant reaction liquid in the reaction vessel, the resultant mixture was stirred for 30 minutes to neutralize the reaction liquid. From the reaction liquid, the resultant precipitated crystals were separated by filtration. A 1,2-propanediol monohydroxydodecyl ether mixture was obtained in an amount of 432.0 g (yield: 97.3%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07138365B2
出典データセットuspto-grants-2006_11
ORD IDord-23de3c30c0e944e5a2495e855daa4a87
出典メモuspto-grants-2006_11