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HRID 721997作成日:2026年10月24日

Propylene Glycol → 1,2-Propanediol ethyleneglycol monohydroxyoctadecyl ether

https://huagongshe.com/ja/reaction/721997

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-EpoxydodecaneHCID 17858—
反応物1,2-EpoxyoctadecaneHCID 23872—
反応物Sodium BicarbonateHCID 516892—
反応物Calcium ChlorideHCID 5284359—
生成物1,2-Propanediol ethyleneglycol monohydroxyoctadecyl etherHCID 13172606096.7%

反応条件

温度72.5 °C

反応手順

Separately, a 1.0 liter mixing vessel equipped with a calcium chloride-containing tube was charged with 402.7 g (1.50 moles) of 1,2-epoxyoctadecane. While the charged 1,2-epoxyoctadecane was stirred at room temperature, a concentrated sulfuric acid was gradually dropped in an amount of 2.7 g (0.027 mole) into 1,2-epoxyoctadecane. 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 70 to 75° C. over a time of 2 hours. Then the reaction of the mixture was carried out at a temperature of 70 to 75° C. for one hour. After the exhaustion of the starting material, namely 1,2-epoxydodecane 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 precipitated crystals were separated by filtration. A 1,2-propanediol monohydroxyoctadecyl ether mixture was obtained in an amount of 510.9 g (yield: 96.7%).

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-82ca558d372e412aa7e838b3c0f07146
出典メモuspto-grants-2006_11