反応 #2808
ord-f82b850c17b44c82bd3c88a18c85d0b3
反応方程式
反応物
試薬
反応条件
後処理
- 1温度cool 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
- 6洗浄wash with 5% sulfuric acid (40 mL) and saturated sodium hydrogen carbonate (40 mL)
- 7抽出Back extract with methylene chloride (100 mL)
- 8洗浄wash with brine (30 mL)
- 9乾燥dry (Na2SO4)
- 10その他Evaporate the solvent in vacuo
- 11その他purify by silica gel chromatography (2:1 hexane/ethyl acetate)
実験手順
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%).