反应 #684974
ord-90661967ac1541b688649dc2500118ba
反应方程式
ethyl acetate
Trifluoroacetic acid
compound
2-(4-Bromo-2-fluorobenzyl)-3-(methoxymethoxy)pyridine
sodium hydrogencarbonate
→
title compound
收率 84.1%
2-(4-Bromo-2-fluorobenzyl)-3-pyridinol
收率 84.1%
反应物
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1workup.ADDITIONwas added
- 2洗涤The ethyl acetate layer was washed with saturated brine
- 3浓缩concentrated under reduced pressure
- 4其他The residue was purified by silica gel column chromatography
实验过程
Trifluoroacetic acid (1 ml) was added to the compound of Example B244 (134 mg, 0.411 mmol) in methylene chloride (4 ml), and this reaction mixture was stirred at room temperature overnight. After neutralizing the mixture with saturated aqueous sodium hydrogencarbonate, ethyl acetate was added. The ethyl acetate layer was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (97.5 mg).