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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2695생성일: 2026년 10월 23일

Water → 3-Cyano-1-diethoxyphosphinylpropanesulfonic acid lithium salt

https://huagongshe.com/ko/reaction/2695

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcrylonitrileHCID 7855—
반응물Lithium (diethoxyphosphoryl)methanesulfonateHCID 23683927—
반응물ButyllithiumHCID 178418339—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물3-Cyano-1-diethoxyphosphinylpropanesulfonic acid lithium saltHCID 88352007—

반응 단계

A suspension of 2.38 g (0.01 mole) of diethoxyphosphinylmethanesulfonate lithium salt (Carretero, et al.; Tetrahedron, 43, 5125 (1987)) in 50 ml of anhydrous tetrahydrofuran is stirred in a -40° bath under a dry nitrogen atmosphere. To this is added n-butyl lithium (4.4 ml of 2.5M solution in hexanes; 0.011 mole) via syringe over 5 minutes. The reaction mixture is allowed to warm to -15° and is stirred at this temperature for about one hour. To it is then added rapidly a solution of 0.53 g (0.01 mole) of acrylonitrile in 3 ml of anhydrous THF. The reaction mixture is stirred for 1 hour at -15° , and is then allowed to warm to room temperature over several hours as the bath warms up. It is stirred at ambient temperature for several hours, and then is quenched by addition of 50 ml of water containing 0.6 g (0.01 mole) of acetic acid. The reaction mixture is concentrated under vacuum on a rotary evaporator to get rid of the THF, and the aqueous layer is extracted with ether to remove some impurities. The water layer is evaporated to dryness under vacuum, and the resulting residue is purified by flash chromatography on silica gel using chloroform/methanol as eluant, to afford 3-cyano-1-diethoxyphosphinylpropanesulfonic acid lithium salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731299
출처 데이터셋uspto-grants-1998_03
ORD IDord-a3dd7bd8f8c04710b88cd5e838b3da7e
출처 메모uspto-grants-1998_03