関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Neodecanoyl chloride | HCID 94502 | — |
| 反応物 | Hydroperoxide, phenylcyclohexyl- | HCID 185715 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-Phenylcyclohexylperoxy neodecanoate | HCID 19981053 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05075495 |
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| 出典データセット | uspto-grants-1991_12 |
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| ORD ID | ord-5a22fc10ee5b40fb927d43002cfa8982 |
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| 出典メモ | uspto-grants-1991_12 |
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