HRID1916824
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 35 °C
PROCEDURE
实验过程
The major product alkene, N-[(1R)-1-((1S)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-phenoxyethyl)pent-4-en-1-yl]-2-methylpropane-2-sulfinamide (160 mg; 0.364 mmol) from Step F, 4-nitrostyrene (220 mg; 1.475 mmol) and Grubbs-II metathesis catalyst (45 mg; 0.053 mmol) were combined in anhydrous methylene chloride (6 ml) and the resulting reaction mixture stirred for 20 hours at 35° C. The crude product solution was concentrated under reduced pressure and the residues purified by silica gel plate chromatography on (20 cm×20 cm×1000 microns) eluted with hexanes and ethyl acetate (2:1 v/v) from which 116 mg of the desired metathesis product was obtained, m/z (ES) 561.22 (M+H)+.
WORKUP
后处理
- customthe resulting reaction mixture
- concentrationThe crude product solution was concentrated under reduced pressure
- customthe residues purified by silica gel plate chromatography on (20 cm×20 cm×1000 microns)
- washeluted with hexanes and ethyl acetate (2:1 v/v) from which 116 mg of the desired metathesis product
- customwas obtained