反应 #684971

ord-61e35bb18f3f4c16ac066b8c62c662e6

反应方程式

O=C(O)C(F)(F)F
Trifluoroacetic acid
CCCCc1ccc(Cc2ncccc2OCOC)cc1
compound
CCCCc1ccc(Cc2ncccc2OCOC)cc1
2-(4-Butylbenzyl)-3-(methoxymethoxy)pyridine
O=C([O-])O.[Na+]
sodium hydrogencarbonate
CCOC(C)=O
ethyl acetate
CCCCc1ccc(Cc2ncccc2O)cc1
title compound
收率 88.8%
CCCCc1ccc(Cc2ncccc2O)cc1
2-(4-Butylbenzyl)-3-pyridinol
收率 88.8%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤the reaction mixture was washed with saturated brine
  2. 2
    浓缩concentrated under reduced pressure
  3. 3
    其他The residue was purified by silica gel column chromatography

实验过程

Trifluoroacetic acid (1 ml) was added to a solution of the compound of Example B229 (256 mg, 0.849 mmol) in methylene chloride (5 ml), and this reaction mixture was stirred at room temperature overnight. After a saturated aqueous sodium hydrogencarbonate solution and ethyl acetate were added, the reaction mixture was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (182 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07897387B2uspto-grants-2011_03