돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542312생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/542312

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물DiisopropylamineHCID 7912—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 2-cyanoethyl(diethoxymethyl)phosphinateHCID 10037677—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Ethyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinateHCID 14362814—

반응 단계

The starting material may be prepared as follows: 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04656298
출처 데이터셋uspto-grants-1987_04
ORD IDord-f0cb1cef15bf4665bbe0513cc7ea9110
출처 메모uspto-grants-1987_04