반응 #7553
ord-418ee189789f42de93dac3320c3963b2
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후처리
- 1workup.ADDITIONby adding
- 2온도After the reaction mixture was cooled
- 3기타the organic layer was separated
- 4세척The organic layer was washed with a saturated aqueous sodium chloride solution
- 5건조dried over anhydrous magnesium sulfate
- 6workup.DISTILLATIONdistilled under reduced pressure
- 7기타to remove the solvent
- 8기타The residue was purified by a column chromatography (eluent; chloroform:methanol=75:1)
실험 절차
In a mixture of 0.4 mL of toluene and 7 mL of a 50% (W/V) aqueous sodium hydroxide solution was suspended 0.54 g of 2-(1-benzothiophen-5-yl)-1-ethanol, followed by adding thereto 1.45 g of 1-(3-chloropropyl)-3-(trityloxy)azetidine oxalate and 0.03 g of tetra-n-butylammonium bromide, and the resulting mixture was refluxed for 7 hours. After the reaction mixture was cooled, water and toluene were added thereto and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=75:1) to obtain 0.59 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-(trityloxy)azetidine as a light-yellow oil.