반응 #2808
ord-f82b850c17b44c82bd3c88a18c85d0b3
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반응물
시약
반응 조건
후처리
- 1온도cool in an ice bath
- 2workup.STIRRINGStir for 22 hours at 5° C.
- 3workup.WAITat room temperature for 1.5 hours
- 4workup.ADDITIONadd 0.6 times all reagents
- 5workup.STIRRINGstir at room temperature overnight
- 6세척wash with 5% sulfuric acid (40 mL) and saturated sodium hydrogen carbonate (40 mL)
- 7추출Back extract with methylene chloride (100 mL)
- 8세척wash with brine (30 mL)
- 9건조dry (Na2SO4)
- 10기타Evaporate the solvent in vacuo
- 11기타purify by silica gel chromatography (2:1 hexane/ethyl acetate)
실험 절차
Dissolve 2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(2-vinyl-phenyl)-propionic acid (2.47 g, 7.69 mmol) in tetrahydrofuran (35 mL) and cool in an ice bath. Treat with pyridine (1.6 mL, 20 mmol) and 2-(trimethylsilyl)ethanol (2.3 mL, 16 mmol). Stir for 30 minutes and add 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) (2.21 g, 11.5 mmol). Stir for 22 hours at 5° C., then at room temperature for 1.5 hours. Cool to 0° C., add 0.6 times all reagents and stir at room temperature overnight. Dilute with ethyl acetate (150 mL), wash with 5% sulfuric acid (40 mL) and saturated sodium hydrogen carbonate (40 mL). Back extract with methylene chloride (100 mL), wash with brine (30 mL) and dry (Na2SO4). Evaporate the solvent in vacuo and purify by silica gel chromatography (2:1 hexane/ethyl acetate) to give the title compound (2.61 g, 81%).