反应 #833526
ord-de40f9576c934f56ac948ce2cd1a2c83
反应方程式
3-[(6-bromohexyloxy)methyl]-3-methyloxetane
ethyl 4-hydroxybenzoate
potassium carbonate
dimethyl formamide
→
ethyl 4-[6-(2-methyloxetane-3-ylmetoxy)hexyloxy)benzoate
收率 80.6%
反应物
试剂
无
溶剂
反应条件
温度
90°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他to terminate
- 2其他the reaction
- 3萃取after extraction with ethyl acetate
- 4萃取the liquid extract
- 5洗涤was washed with an aqueous solution of 2N-sodium hydroxide and water successively
- 6干燥the organic layer was dried over anhydrous magnesium sulfate
- 7其他The residues obtained
- 8workup.DISTILLATIONby distilling off the solvent
- 9其他were purified on silica gel chromatography (toluene/ethyl acetate=8/2)
实验过程
A mixture of 3-[(6-bromohexyloxy)methyl]-3-methyloxetane (84 g), ethyl 4-hydroxybenzoate (50 g), potassium carbonate (50 g) and dimethyl formamide (600 mL) was stirred at 90° C. for 4 hours. Water was added to the reaction mixture to terminate the reaction and, after extraction with ethyl acetate, the liquid extract was washed with an aqueous solution of 2N-sodium hydroxide and water successively, and the organic layer was dried over anhydrous magnesium sulfate. The residues obtained by distilling off the solvent were purified on silica gel chromatography (toluene/ethyl acetate=8/2), to obtain ethyl 4-[6-(2-methyloxetane-3-ylmetoxy)hexyloxy)benzoate (85 g).