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HRID 5170作成日:2026年10月23日

Chloroform → Ethyl 3-oxobutyl(diethoxymethyl)phosphinate

https://huagongshe.com/ja/reaction/5170

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物Methyl vinyl ketoneHCID 6570—
反応物HCID 178418659HCID 178418659—
溶媒WaterHCID 962—
生成物Ethyl 3-oxobutyl(diethoxymethyl)phosphinateHCID 14362820—

反応条件

温度50 °C

反応手順

15.0 g of ethyl trimethylsilyl(diethoxymethyl)phosphonite are added dropwise to a stirred solution of 3.9 g of methyl vinyl ketone under an atmosphere of nitrogen at room temperature. The mixture is then heated to 50° C. for a period of 1 hour. The mixture is then allowed to cool to room temperature, 25 ml of chloroform is then added followed by 10 ml water and this mixture is vigorously stirred for a period of 0.5 h. The organic layer is then separated, dried over magnesium sulphate and concentrated under reduced pressure and the crude product distilled under reduced pressure to give ethyl 3-oxobutyl(diethoxymethyl)phosphinate, b.p. 130°-135° C./0.02 mbar, 31P=+45.3 ppm (CDCl3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05243062
出典データセットuspto-grants-1993_09
ORD IDord-30eae213606d47d0a395349b420efeef
出典メモuspto-grants-1993_09