反应详情

温度

90 °C

25 mg of copper iodide, 44 mg of bis-(triphenylphosphine)-palladium dichloride, 0.30 ml triethylamine and finally 0.14 ml of trimethylsilylacetylene are added under argon to a solution of 0.32 g 1-chloro-4-(β-D-glucopyranos-1-yl)-2-[4-(trifluoromethylsulfonyloxy)-benzyl]-benzene in 3 ml of dimethylformamide. The flask is tightly sealed and stirred for 8 h at 90° C. Then another 25 mg of bis-(triphenylphosphine)-palladium dichloride and 0.1 ml trimethylsilylacetylene are added, and the solution is stirred for a further 10 h at 90° C. Then aqueous sodium hydrogen carbonate solution is added, the mixture is extracted three times with ethyl acetate, and the combined organic phases are dried over sodium sulfate. After the solvent is removed the residue is dissolved in 5 ml of methanol and combined with 0.12 g potassium carbonate. The mixture is stirred for 1 h at ambient temperature and then neutralised with 1 M hydrochloric acid. Then the methanol is evaporated off, the residue is combined with aqueous sodium chloride solution and extracted with ethyl acetate. The organic extracts collected are dried over sodium sulfate, and the solvent is removed. The residue is chromatographed on silica gel (dichloromethane/methanol 1:0→5:1).

1. customThe flask is tightly sealed
2. stirringthe solution is stirred for a further 10 h at 90° C
3. extractionthe mixture is extracted three times with ethyl acetate
4. dry with materialthe combined organic phases are dried over sodium sulfate
5. customAfter the solvent is removed the residue
6. dissolutionis dissolved in 5 ml of methanol
7. stirringThe mixture is stirred for 1 h at ambient temperature
8. customThen the methanol is evaporated off
9. extractionextracted with ethyl acetate
10. customThe organic extracts collected
11. dry with materialare dried over sodium sulfate
12. customthe solvent is removed
13. customThe residue is chromatographed on silica gel (dichloromethane/methanol 1:0→5:1)