反应 #2808

ord-f82b850c17b44c82bd3c88a18c85d0b3

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cool in an ice bath
  2. 2
    workup.STIRRINGStir for 22 hours at 5° C.
  3. 3
    workup.WAITat room temperature for 1.5 hours
  4. 4
    workup.ADDITIONadd 0.6 times all reagents
  5. 5
    workup.STIRRINGstir at room temperature overnight
  6. 6
    洗涤wash with 5% sulfuric acid (40 mL) and saturated sodium hydrogen carbonate (40 mL)
  7. 7
    萃取Back extract with methylene chloride (100 mL)
  8. 8
    洗涤wash with brine (30 mL)
  9. 9
    干燥dry (Na2SO4)
  10. 10
    其他Evaporate the solvent in vacuo
  11. 11
    其他purify by silica gel chromatography (2:1 hexane/ethyl acetate)

实验过程

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%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05731306uspto-grants-1998_03