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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622904생성일: 2026년 10월 27일

Diisopropylamine → Ethyl 2-(4-methylphenyl)-3-nitropropyl(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/622904

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물Ammonium ChlorideHCID 25517—
반응물1-Methyl-4-(2-nitroethenyl)benzeneHCID 286735—
반응물Ethyl(diethoxymethyl)methylphosphinateHCID 13764418—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Ethyl 2-(4-methylphenyl)-3-nitropropyl(diethoxymethyl)phosphinateHCID 14362829—

반응 단계

To a solution of 8.7 g of diisopropylamine in 40 ml of tetrahydrofuran at -78° C. under an atmosphere of nitrogen are added 53.6 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 15.0 g of ethyl(diethoxymethyl)methylphosphinate in 20 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 11.6 g of 4-methyl-β-nitrostyrene in 20 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-(4-methylphenyl)-3-nitropropyl(diethoxymethyl)phosphinate as a viscous oil, 31P=+42.5 and +42.1 ppm (CDCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04772738
출처 데이터셋uspto-grants-1988_09
ORD IDord-6773bad7f9b84ab88ef0798975cbdf70
출처 메모uspto-grants-1988_09