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HRID 5185作成日:2026年10月25日

Benzyl Bromide → Ethyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/5185

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物DiisopropylamineHCID 7912—
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl 2-cyanoethyl(diethoxymethyl)phosphinateHCID 10037677—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Ethyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinateHCID 14362814—

反応手順

To a solution of 0.97 g of diisopropylamine in 40 ml of tetrahydrofuran at -78° C. under an atmosphere of nitrogen are added 6.0 ml of a 1.6M solution of n-butyllithium in hexane. This solution is then stirred for a period of 10 minutes at this temperature, after which time a solution of 2.0 g of ethyl 2-cyanoethyl(diethoxymethyl)phosphinate in 10 ml of tetrahydrofuran is added. This mixture is then stirred for a period of 1 hour at -78° C. after which time a solution of 1.4 g of benzyl bromide in 10 ml of tetrahydrofuran is introduced. This mixture is then allowed to warm to room temperature when 40 ml of a saturated ammonium chloride solution is added. The aqueous layer is then extracted with 2×25 ml of diethyl ether and the organic extracts are combined and dried over magnesium sulphate. The solvent is then evaporated under reduced pressure and the crude product chromatographed on silica gel using ethyl acetate as an eluent to give ethyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinate as a viscous oil, 31P=+40.7 and +40.5 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-856eab2a0560410681b793d4b1b773fd
出典メモuspto-grants-1993_09