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HRID 1461587作成日:2026年10月25日

Benzene → 1-Phenylcyclohexylperoxy neodecanoate

https://huagongshe.com/reaction/1461587

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Potassium HydroxideHCID 14797—
反応物Neodecanoyl chlorideHCID 94502—
反応物Hydroperoxide, phenylcyclohexyl-HCID 185715—
溶媒WaterHCID 962—
生成物1-Phenylcyclohexylperoxy neodecanoateHCID 19981053—

反応条件

温度10 °C

反応手順

In a four-necked flask of 200 ml provided with a stirrer was charged 33.7 g of an aqueous solution of 30% potassium hydroxide, to which was added a mixture of 22.1 g of 95% 1-phenylcyclohexyl hydroperoxide and 30 g of benzene while the liquid temperature was maintained at 10° C. with stirring. Furthermore, 19.1 g of neodecanoyl chloride was added dropwise over 7 minutes while the liquid temperature was maintained at 15° C. with stirring. After the liquid temperature was raised to 25° C. and the stirring was continued for 2 hours, 40 g of cold water was added and further the stirring was made for 5 minutes. The water phase was separated and washed with an aqueous solution of 40 g of 5% sodium hydroxide and further with water three times. The solution was dried on magnesium sulfate anhydride and benzene was removed off under vacuum to obtain 24.0 g of a desired compound as a light yellow liquid. This compound had an active oxygen amount of 4.20%, a purity of 91% through calculation and a yield of 63 mol %.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05075495
出典データセットuspto-grants-1991_12
ORD IDord-5a22fc10ee5b40fb927d43002cfa8982
出典メモuspto-grants-1991_12