반응 #2791
ord-a3dd7bd8f8c04710b88cd5e838b3da7e
반응 방정식
반응 조건
후처리
- 1온도to warm to -15°
- 2workup.STIRRINGis stirred at this temperature for about one hour
- 3workup.STIRRINGThe reaction mixture is stirred for 1 hour at -15°
- 4workup.STIRRINGIt is stirred at ambient temperature for several hours
- 5농축The reaction mixture is concentrated under vacuum on a rotary evaporator
- 6기타to get rid of the THF
- 7추출the aqueous layer is extracted with ether
- 8기타to remove some impurities
- 9기타The water layer is evaporated to dryness under vacuum
- 10기타the resulting residue is purified by flash chromatography on silica gel
실험 절차
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.