反应 #1755495
ord-c6e8416f1a49444fb00b75f9d471775f
反应方程式
4-[(4-methoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
potassium carbonate
Iodomethane
→
4-[(4-methoxyphenyl)methyl]-1,5-dimethyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)pyrazole
收率 21.7%
反应物
试剂
无
反应条件
温度
75°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1过滤The reaction mixture was filtered through Celite®
- 2其他the solvent of the filtrate was removed under reduced pressure
- 3其他The residue was purified by preparative thin layer chromatography on silica gel (developing solvent: benzene/acetone=2/1)
实验过程
A suspension of 4-[(4-methoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole (18 mg), potassium carbonate (14 mg) and Iodomethane (4.7 mg) in acetonitrile (2 mL) was stirred at 75° C. overnight. The reaction mixture was filtered through Celite®, and the solvent of the filtrate was removed under reduced pressure. The residue was purified by preparative thin layer chromatography on silica gel (developing solvent: benzene/acetone=2/1) to give 4-[(4-methoxyphenyl)methyl]-1,5-dimethyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)pyrazole (4 mg).